Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
G/A | Ancestral: G | Ambiguity code: R
Location

Chromosome 7:94585227 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

7:g.94585227G>A

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 8 transcripts and has 270 sample genotypes.

Variant displays