Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 17:32584435 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

17:g.32584435A>C

Genotyping chips

This variation has assays on: Illumina_ImmunoChip

Variation displays