Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.01 (G)
Location

Chromosome 22:23521698 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

22:g.23521698C>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays