Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.45 (G)
Location

Chromosome 11:116837304 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17249484, rs61758322

HGVS names

This variant has 9 HGVS names - Show

About this variant

This variant overlaps 10 transcripts, 1 regulatory feature, has 2533 sample genotypes and is mentioned in 5 citations.

Variant displays