Original source

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

Alleles
G/T | Ancestral: T | Ambiguity code: K | MAF: 0.23 (T)
Location

Chromosome 3:58427942 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs3181868, rs1126698

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_ImmunoChip, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays