Original source

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

Alleles
A/C | Ancestral: T | Ambiguity code: M | MAF: 0.45 (A)
Location

Chromosome 8:94248848 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

8:g.94248848A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays