Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.07 (C)
Location

Chromosome 1:247922126 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.247922126A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays