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 14 transcripts and has 2776 sample genotypes.

Variant displays