Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.06 (A)
Location

Chromosome 2:118848184 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.118848184A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays