Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.48 (A)

Chromosome 11:128773658 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58299908, rs59604667

HGVS names

This variant has 7 HGVS names - Show

Genotyping chips

This variant has assays on 8 chips - Show

About this variant

This variant overlaps 7 transcripts and has 3970 sample genotypes.

Variant displays