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
C/A | Ancestral: C | Ambiguity code: M
Location

Chromosome 16:50774480 (forward strand) | View in location tab

Most severe consequence

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays