Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.05 (A)

Chromosome 11:116835331 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs17249442

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 12 transcripts, has 2528 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays