Variant (rsID / SNP)
rs3748570
rs3748570 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to NES. Location: chromosome 1, position 156,640,156. The table records no clinical significance for this variant.
Reference-table entries
NESNot classified
- Variant type
- missense_variant
- Chromosome / position
- 1:156640156
- HGVS
- NM_006617.2,c.3824C>T,p.Pro1275Leu
- Allele change
- Missense_P1275L
Associated conditions / phenotypes
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.