Original source

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

Alleles
A/C | Ancestral: C | Ambiguity code: M | MAF: 0.07 (A)
Location

Chromosome 22:37212536 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs57725855

This variation has 7 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_HumanOmni2.5, Illumina_HumanOmni5

Variation displays