Original source

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

Alleles
A/T | Ancestral: T | Ambiguity code: W | MAF: 0.28 (A)
Location

Chromosome 9:129663952 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

9:g.129663952A>T

Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 1 transcript and has 2510 sample genotypes.

Variant displays