Original source

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

G/C | Ancestral: C | Ambiguity code: S | MAF: 0.03 (G)

Chromosome 12:11687255 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs862790, rs60068750, rs1210184

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 4 transcripts and has 1107 individual genotypes.

Variation displays