Original source

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

Alleles
T/A|Ancestral: A|Ambiguity code: W|MAF: 0.01 (A)
Location

Chromosome 5:161845762 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

5:g.161845762T>A

About this variant

This variant overlaps 9 transcripts and has 2504 sample genotypes.

Variant displays