Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.36 (A)
Location

Chromosome 20:59298524 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms
HGVS name

20:g.59298524A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays