Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.30 (G)
Location

Chromosome 1:33338603 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs58655647

HGVS name

1:g.33338603G>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays