Original source

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

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

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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