Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: < 0.01 (A)
Location

Chromosome 7:22725249 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.22725249C>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays