Variant (rsID / SNP)
rs6131
rs6131 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to SELP. Location: chromosome 1, position 169,580,885. The table records no clinical significance for this variant.
Reference-table entries
SELPNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:169580885
- HGVS
- NM_003005.4,c.992G>A,p.Ser331Asn
- Allele change
- Missense_S331N
Associated conditions / phenotypes
Myocardial Infarction|Hypertension, Essential|Heart Disease|Coronary Heart Disease 1
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.