SLC12A6 Chromosome 15

Solute carrier family 12 member 6
224 variants 224 Health Risk

Upload your DNA to see your personal genotypes for variants in SLC12A6.

What This Gene Does
This gene is a member of the K-Cl cotransporter (KCC) family. K-Cl cotransporters are integral membrane proteins that lower intracellular chloride concentrations below the electrochemical equilibrium potential. The proteins encoded by this gene are activated by cell swelling induced by hypotonic conditions. Alternate splicing results in multiple transcript variants encoding different isoforms. Mutations in this gene are associated with agenesis of the corpus callosum with peripheral neuropathy. [provided by RefSeq, Jul 2008]
Gene Info
Gene Group
Solute carrier family 12
Locus Type
gene with protein product
Location
15q14
Ensembl
ENSG00000140199
Associated Conditions (16)
Agenesis of the corpus callosum with peripheral neuropathy
Charcot-Marie-Tooth disease
Inborn genetic diseases
SLC12A6-related disorder
axonal
IIa 2II
Peripheral neuropathy
See cases
Melanoma
Usher syndrome type 1C
Hypertelorism
Corpus callosum
agenesis of
Clinodactyly of the 5th finger
Abnormal facial shape
Low-set ears
Key Variants
RS1005396685
Conflicting classifications of pathogenicity
Health Risk
RS117540484
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
Health Risk
RS121908429
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, Charcot-Marie-Tooth disease, Agenesis of the corpus callosum with peripheral neuropathy
Health Risk
RS142496698
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
Health Risk
RS145615604
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, Inborn genetic diseases, Agenesis of the corpus callosum with peripheral neuropathy
Health Risk
RS149640638
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
Health Risk
RS150751809
Conflicting classifications of pathogenicity
SLC12A6-related disorder, Charcot-Marie-Tooth disease, axonal
Health Risk
RS17236798
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, SLC12A6-related disorder, Agenesis of the corpus callosum with peripheral neuropathy
Health Risk
RS1894227805
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
Health Risk
RS199945338
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, Charcot-Marie-Tooth disease, axonal
Health Risk
RS200110068
Conflicting classifications of pathogenicity
Health Risk
RS200544602
Conflicting classifications of pathogenicity
Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
Health Risk
All Variants (224)
RSID Category Clinical Significance Conditions
RS1005396685 Health Risk Conflicting classifications of pathogenicity
RS117540484 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS121908429 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Charcot-Marie-Tooth disease, Agenesis of the corpus callosum with peripheral neuropathy
RS142496698 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS145615604 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Inborn genetic diseases, Agenesis of the corpus callosum with peripheral neuropathy
RS149640638 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS150751809 Health Risk Conflicting classifications of pathogenicity SLC12A6-related disorder, Charcot-Marie-Tooth disease, axonal
RS17236798 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, SLC12A6-related disorder, Agenesis of the corpus callosum with peripheral neuropathy
RS1894227805 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS199945338 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Charcot-Marie-Tooth disease, axonal
RS200110068 Health Risk Conflicting classifications of pathogenicity
RS200544602 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS201062811 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Inborn genetic diseases, SLC12A6-related disorder
RS2509782899 Health Risk Conflicting classifications of pathogenicity Charcot-Marie-Tooth disease, axonal, IIa 2II
RS35855196 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS369793136 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS370477960 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS375887656 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, SLC12A6-related disorder, Agenesis of the corpus callosum with peripheral neuropathy
RS376575991 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS562984167 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Inborn genetic diseases, Agenesis of the corpus callosum with peripheral neuropathy
RS75235010 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Inborn genetic diseases, Agenesis of the corpus callosum with peripheral neuropathy
RS753466496 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS763835588 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS764272139 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Inborn genetic diseases, Agenesis of the corpus callosum with peripheral neuropathy
RS770370694 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS770742608 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS77122016 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, SLC12A6-related disorder, Agenesis of the corpus callosum with peripheral neuropathy
RS773294017 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS774081365 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS778821191 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Inborn genetic diseases, SLC12A6-related disorder
RS779390859 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS886051056 Health Risk Conflicting classifications of pathogenicity Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1057516271 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1057516337 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Charcot-Marie-Tooth disease, axonal
RS1057516378 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1057516435 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1057516752 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1057516898 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1057516925 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1057516969 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Charcot-Marie-Tooth disease, axonal
RS1057517109 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1057517334 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1182209513 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1444227608 Health Risk Likely pathogenic
RS1555376682 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1555376688 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, SLC12A6-related disorder, Agenesis of the corpus callosum with peripheral neuropathy
RS1555376818 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1555377252 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1555377971 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
RS1555378707 Health Risk Likely pathogenic Agenesis of the corpus callosum with peripheral neuropathy, Agenesis of the corpus callosum with peripheral neuropathy
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