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Variant (rsID / SNP)

rs172917

ASTN1

rs172917 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to ASTN1. Location: chromosome 1, position 176,992,553. The table records no clinical significance for this variant.

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Reference-table entries

ASTN1Not classified
Variant type
synonymous_variant
Chromosome / position
1:176992553
HGVS
NM_001364856.2,c.1425T>C,p.Cys475Cys
Allele change
Synonymous_C475C

Associated conditions / phenotypes

Alcohol Dependence|Major Affective Disorder 8|Major Affective Disorder 9|Substance Abuse|Bipolar Disorder

Public references

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.