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 12:117208066 (forward strand) | View in location tab

Most severe consequence
 
Downstream gene variant
HGVS name

12:g.117208066G>A

Genotyping chips

This variant has assays on: Illumina_Human1M-duo

About this variant

This variant overlaps 2 transcripts.

Variant displays