Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.36 (C)

Chromosome 3:38770674 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs10290125, rs57130846

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_Cardio-Metabo_Chip, Affy GenomeWideSNP_6.0

About this variant

This variant overlaps 1 transcript and has 3966 sample genotypes.

Variant displays