Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | 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

This variant has assays on 4 chips - click the plus to show

About this variant

This variant overlaps 5 transcripts, 1 regulatory feature, has 2544 sample genotypes, is associated with 1 phenotype and is mentioned in 6 citations.

Variant displays