Original source

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

Alleles
A/G|Ancestral: A|Ambiguity code: R|MAF: 0.21 (G)
Location

Chromosome 11:27690834 (forward strand)|View in location tab

Most severe consequence
 
Intron variant
Evidence status

Synonyms

Archive dbSNP rs17429365, rs57659753

HGVS names

This variant has 21 HGVS names - Show

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 20 transcripts, has 3761 sample genotypes, is associated with 1 phenotype and is mentioned in 2 citations.

Variant displays