Original source

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

Alleles
A/T|Ambiguity code: W|MAF: 0.37 (A)
Location

Chromosome 11:18264227 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs60261995, rs52832266

HGVS name

11:g.18264227A>T

Genotyping chips

This variant has assays on 4 chips - Show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 2776 sample genotypes, is associated with 1 phenotype and is mentioned in 7 citations.

Variant displays