Original source

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

G/C | Ancestral: G | Ambiguity code: S | MAF: 0.27 (C)

Chromosome 13:33022117 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs560427

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

About this variant

This variant overlaps 2 transcripts and has 1104 individual genotypes.

Variation displays