Original source

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

Alleles
G/C/T | Ancestral: T | Ambiguity code: B | MAF: 0.45 (G)
Location

Chromosome 1:20650956 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

This variation has 10 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays