Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.46 (A)
Location

Chromosome 11:69810962 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58874829

This variation has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 2508 individual genotypes.

Variation displays