Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

C/G | Ancestral: C | Ambiguity code: S | MAF: 0.23 (C)

Chromosome 12:7694464 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs5013153

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 1103 individual genotypes.

Variation displays