Original source

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

Alleles
C/G | Ancestral: G | Ambiguity code: S | MAF: 0.05 (G)
Location

Chromosome 13:33014800 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs36217257, rs56874385

HGVS name

13:g.33014800C>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays