Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.47 (G)
Location

Chromosome 12:105213958 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 2507 individual genotypes.

Variation displays