Original source

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

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

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

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs60261995, rs52832266

HGVS name


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