Original source

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

Alleles
C/A | Ancestral: C | Ambiguity code: M | MAF: 0.04 (A)
Location

Chromosome 11:635796 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117321595

HGVS name

11:g.635796C>A

Genotyping chips

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

Variation displays