Original source

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

Alleles
T/G|Ancestral: T|Ambiguity code: K|MAF: 0.05 (G)
Location

Chromosome 11:116835452 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs17249449

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 12 transcripts, has 2528 sample genotypes and is mentioned in 2 citations.

Variant displays