Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: < 0.01 (A)
Location

Chromosome 4:53376015 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

4:g.53376015G>A

About this variant

This variant overlaps 9 transcripts and has 2505 individual genotypes.

Variation displays