Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.19 (C)
Location

Chromosome 11:635569 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.635569A>C

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays