Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.28 (A)
Location

Chromosome 9:139583478 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59741514

HGVS name

9:g.139583478A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays