Original source

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

Alleles
C/A | Ancestral: T | Ambiguity code: M | MAF: 0.10 (A)
Location

Chromosome 1:39623144 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.39623144C>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_Human1M-duo

Variation displays