Original source

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

A/G | Ancestral: G | Ambiguity code: R | MAF: 0.43 (G)

Chromosome 7:128828479 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status


Archive dbSNP rs60616659, rs3807130

HGVS names

This variant has 2 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 3 transcripts and has 2602 sample genotypes.

Variant displays