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
A/G/T | Ancestral: A | Ambiguity code: D | MAF: 0.06 (G)
Location

Chromosome 12:123254538 (forward strand) | View in location tab

Most severe consequence
Evidence status

This variation has 6 HGVS names - click the plus to show

This variation has assays on 5 chips - click the plus to show

Variation displays