Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.26 (G)
Location

Chromosome 6:111186193 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59346483, rs375239

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

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_HumanOmni5, Illumina_1M-duo

Variation displays