Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y
Location

Chromosome 20:46708523 (forward strand) | View in location tab

Most severe consequence
 
Upstream gene variant
HGVS name

20:g.46708523T>C

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts and 2 regulatory features.

Variant displays