Original source

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

G/A/C | Ancestral: G | Ambiguity code: V | MAF: 0.11 (A)

Chromosome 19:33495473 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs388725, rs253672, rs835582

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 14 transcripts and has 2774 sample genotypes.

Variant displays