Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K | MAF: 0.38 (G)
Location

Chromosome 13:27620912 (forward strand) | View in location tab

Co-located

with dbSNP rs200073353 (T/-)

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs1745501, rs58761937

This variation has 3 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays