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: 0.24 (A)
Location

Chromosome 19:50515560 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57829586

HGVS name

19:g.50515560A>G

Genotyping chips

This variation has assays on: Illumina_1M-duo

Variation displays