Original source

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

C/G | Ancestral: G | Ambiguity code: S | MAF: 0.22 (G)

Chromosome 19:33390741 (forward strand) | View in location tab


with dbSNP rs112977316 (C/-)

Most severe consequence
Intron variant
Evidence status

HGVS names

This variant has 5 HGVS names - Show

About this variant

This variant overlaps 7 transcripts and has 2507 sample genotypes.

Variant displays