Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A | Ancestral: G | Ambiguity code: R

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


with dbSNP rs62790561 (G/-)

Most severe consequence
Intron variant
HGVS names

This variant has 8 HGVS names - Show

Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 14 transcripts.

Variant displays