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 12:56472294 (forward strand) | View in location tab

Most severe consequence
HGVS name

12:g.56472294G>A

Variation displays