Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.43 (A)
Location

Chromosome 17:7185062 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs222845, rs59378065

This variation has 4 HGVS names - click the plus to show

Genotyping chips

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

Variation displays