Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 10:103823135 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.103823135A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5

Variation displays