Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.20 (A)

Chromosome 6:111166487 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs9285405, rs59470130

HGVS names

This variant has 3 HGVS names - Show

Genotyping chips

This variant has assays on 7 chips - Show

About this variant

This variant overlaps 2 transcripts and has 3838 sample genotypes.

Variant displays