SNX10 Chromosome 7

Sorting nexin 10
15 variants 15 Health Risk

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What This Gene Does
This gene encodes a member of the sorting nexin family. Members of this family contain a phox (PX) domain, which is a phosphoinositide binding domain, and are involved in intracellular trafficking. This protein does not contain a coiled coil region, like some family members. This gene may play a role in regulating endosome homeostasis. Alternative splicing results in multiple transcript variants. [provided by RefSeq, Dec 2010]
Gene Info
Gene Group
Sorting nexins
Locus Type
gene with protein product
Location
7p15.2
Ensembl
ENSG00000086300
Associated Conditions (3)
Inborn genetic diseases
Autosomal recessive osteopetrosis 8
Gastric cancer
Key Variants
All Variants (15)
RSID Category Clinical Significance Conditions
RS149177634 Health Risk Conflicting classifications of pathogenicity Inborn genetic diseases, Inborn genetic diseases
RS2536153141 Health Risk Likely pathogenic —
RS2536153865 Health Risk Likely pathogenic Autosomal recessive osteopetrosis 8, Autosomal recessive osteopetrosis 8
RS771038257 Health Risk Likely pathogenic —
RS775298474 Health Risk Likely pathogenic —
RS776348160 Health Risk Likely pathogenic Gastric cancer, Gastric cancer
RS1788391157 Health Risk Pathogenic —
RS2128024652 Health Risk Pathogenic —
RS2536141413 Health Risk Pathogenic —
RS377321694 Health Risk Pathogenic —
RS398123011 Health Risk Pathogenic Autosomal recessive osteopetrosis 8, Autosomal recessive osteopetrosis 8
RS587777490 Health Risk Pathogenic Autosomal recessive osteopetrosis 8, Autosomal recessive osteopetrosis 8
RS753014293 Health Risk Pathogenic —
RS968119159 Health Risk Pathogenic —
RS1353879401 Health Risk Pathogenic/Likely pathogenic Autosomal recessive osteopetrosis 8, Autosomal recessive osteopetrosis 8
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