Original source

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

Alleles
G/A | Ambiguity code: R | MAF: 0.22 (A)
Location

Chromosome 12:106356479 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

12:g.106356479G>A

About this variant

This variant overlaps 2 transcripts and has 2507 individual genotypes.

Variation displays