Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Most severe consequence
HGVS name

4:g.3461931T>A

About this variant

This variant overlaps 4 transcripts and has 270 individual genotypes.

Variation displays