Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.03 (A)
Location

Chromosome 4:3461876 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.3461876G>A

About this variant

This variant overlaps 4 transcripts and has 2504 individual genotypes.

Variation displays