Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.24 (A)
Location

Chromosome 19:51018817 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57829586

HGVS name

19:g.51018817A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays