Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.45 (A)

Chromosome 11:69811923 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58981047

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 2509 sample genotypes.

Variant displays