Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 10:23190792 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

10:g.23190792T>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 1 transcript and has 2504 sample genotypes.

Variant displays