Original source

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

Alleles
A/T|Ancestral: A|Ambiguity code: W
Location

Chromosome 5:161846288 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

5:g.161846288A>T

About this variant

This variant overlaps 9 transcripts and has 269 sample genotypes.

Variant displays