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 12:132636440 (forward strand) | View in location tab

Co-located

with dbSNP rs62790561 (G/-)

Most severe consequence
 
Intron variant

This variant has 8 HGVS names - click the plus to show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts.

Variant displays