Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.40 (C)
Location

Chromosome 1:183585314 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59317509, rs34492544

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