Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.03 (A)
Location

Chromosome 6:111606279 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs412224, rs58935303

HGVS name

6:g.111606279A>G

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_HumanOmni5

Variation displays