Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.07 (A)

Chromosome 7:101125148 (forward strand) | View in location tab

Most severe consequence
Upstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5

About this variant

This variant overlaps 1 transcript, has 2505 sample genotypes and is mentioned in 1 citation.

Variant displays