Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.31 (C)
Location

Chromosome 22:50582239 (forward strand) | View in location tab

Most severe consequence
Evidence status

Clinical significance

Synonyms

Archive dbSNP rs3747275, rs743617, rs5770921

This variation has 11 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays