Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|View in dbSNP

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

Chromosome 17:34257416 (forward strand)|View in location tab

Most severe consequence
 
Downstream gene variant
Evidence status

HGVS name

17:g.34257416A>C

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

Variant displays