Original source

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

Alleles
G/C | Ancestral: G | Ambiguity code: S | MAF: 0.03 (C)
Location

Chromosome 10:73723637 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.73723637G>C

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni5

Variation displays