Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

G/C/T|Ancestral: C|Ambiguity code: B|MAF: 0.12 (G)

Chromosome 19:17403631 (forward strand)|View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs12975139

HGVS names

This variant has 6 HGVS names - Show

About this variant

This variant overlaps 40 transcripts and has 2776 sample genotypes.

Variant displays