Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

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

Chromosome 11:13323464 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58231100

HGVS names

This variant has 15 HGVS names - Show

About this variant

This variant overlaps 14 transcripts, has 2782 sample genotypes and is mentioned in 1 citation.

Variant displays