Original source

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

C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.31 (T)

Chromosome 6:43515061 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs9462901

This variation has 14 HGVS names - click the plus to show

About this variant

This variant overlaps 28 transcripts and has 2507 individual genotypes.

Variation displays