Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.18 (G)

Chromosome 12:11687450 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs862789, rs57190539, rs448980

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

About this variant

This variant overlaps 4 transcripts and has 1118 individual genotypes.

Variation displays