Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.02 (A)
Location

Chromosome 22:40345014 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

22:g.40345014T>A

About this variant

This variant overlaps 10 transcripts and has 2575 sample genotypes.

Variant displays