Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

C/T | Ancestral: T | Ambiguity code: Y | MAF: 0.16 (T)

Chromosome 1:12203862 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs9430686, rs17881572

This variation has 3 HGVS names - click the plus to show

About this variant

This variant overlaps 3 transcripts and has 2672 individual genotypes.

Variation displays