ASNS Chromosome 7

Asparagine synthetase (glutamine-hydrolyzing)
140 variants 140 Health Risk

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

What This Gene Does
The protein encoded by this gene is involved in the synthesis of asparagine. This gene complements a mutation in the temperature-sensitive hamster mutant ts11, which blocks progression through the G1 phase of the cell cycle at nonpermissive temperature. Alternatively spliced transcript variants have been described for this gene. [provided by RefSeq, May 2010]
Associated Conditions (10)
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Inborn genetic diseases
ASNS-related disorder
Neurodevelopmental abnormality
Abnormal cerebral morphology
Spinocerebellar ataxia
autosomal recessive 29
Neurodevelopmental delay
Pancreatic adenocarcinoma
Gastric cancer
Key Variants
RS1140424
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
RS1252577998
Conflicting classifications of pathogenicity
Health Risk
RS1360484422
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
RS146656175
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Inborn genetic diseases, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
RS148111963
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
RS149193118
Conflicting classifications of pathogenicity
Inborn genetic diseases, Inborn genetic diseases
Health Risk
RS1791279467
Conflicting classifications of pathogenicity
Health Risk
RS1792120689
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
RS201432154
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
RS2115608872
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
RS375234125
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
RS61733327
Conflicting classifications of pathogenicity
Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, ASNS-related disorder, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
Health Risk
All Variants (140)
RSID Category Clinical Significance Conditions
RS2484661548 Health Risk Pathogenic
RS2484662674 Health Risk Pathogenic
RS2484681802 Health Risk Pathogenic
RS2484681831 Health Risk Pathogenic
RS2484681925 Health Risk Pathogenic
RS2484682215 Health Risk Pathogenic
RS2484682243 Health Risk Pathogenic
RS2484682376 Health Risk Pathogenic
RS2484697837 Health Risk Pathogenic
RS2484697936 Health Risk Pathogenic
RS2484698074 Health Risk Pathogenic
RS2484698452 Health Risk Pathogenic
RS2484698495 Health Risk Pathogenic
RS2484698591 Health Risk Pathogenic
RS2484698746 Health Risk Pathogenic
RS398122974 Health Risk Pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS752951804 Health Risk Pathogenic
RS767368474 Health Risk Pathogenic
RS769360935 Health Risk Pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS779172263 Health Risk Pathogenic
RS797045307 Health Risk Pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS1166271142 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS1488937281 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS1791584683 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS1791857109 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS2115616730 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS2115654584 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS2484630568 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS373645939 Health Risk Pathogenic/Likely pathogenic ASNS-related disorder, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, ASNS-related disorder
RS373774032 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Inborn genetic diseases, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS398122973 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS398122975 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS747624770 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS750420071 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS757729851 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS759224338 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS769236847 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Neurodevelopmental delay, Pancreatic adenocarcinoma
RS773348232 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS866033169 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
RS948326794 Health Risk Pathogenic/Likely pathogenic Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome, Congenital microcephaly - severe encephalopathy - progressive cerebral atrophy syndrome
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