Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.03 (C)
Location

Chromosome 16:31189448 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.31189448A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays