Original source

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

Alleles
C/G | Ancestral: C | Ambiguity code: S | MAF: 0.33 (G)
Location

Chromosome 17:1400484 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.1400484C>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays