Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W|MAF: 0.19 (T)
Location

Chromosome 6:31617223 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

6:g.31617223T>A

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 8 transcripts, 1 regulatory feature, has 3985 sample genotypes, is associated with 2 phenotypes and is mentioned in 2 citations.

Variant displays