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: 0.33 (A)
Location

Chromosome 13:19956933 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58437569

HGVS name

13:g.19956933A>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays