Original source

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

T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.16 (C)

Chromosome 11:116835627 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs17249456

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 12 transcripts and has 2530 sample genotypes.

Variant displays