This variation has been flagged

Flagged as suspect by dbSNP

Original source

Variants (including SNPs and indels) imported from dbSNP (release 138) | View in dbSNP

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

Chromosome 12:56472299 (forward strand) | View in location tab

Most severe consequence
HGVS name

12:g.56472299G>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays