Original source

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

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

Chromosome 4:3461931 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

4:g.3461931T>A

About this variant

This variant overlaps 4 transcripts and has 270 sample genotypes.

Variant displays