Variant (rsID / SNP)
rs1764391
rs1764391 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to GJA4. Location: chromosome 1, position 35,260,769. The table records no clinical significance for this variant.
Reference-table entries
GJA4Not classified
- Variant type
- missense_variant
- Chromosome / position
- 1:35260769
- HGVS
- NM_002060.3,c.955C>T,p.Pro319Ser
- Allele change
- Missense_P319S
Associated conditions / phenotypes
Myocardial Infarction|Acute Myocardial Infarction|Coronary Heart Disease 1|Stroke, Ischemic|Heart Disease|Polycystic Ovary Syndrome
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.