Original source

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

Alleles
C/G|Ancestral: C|Ambiguity code: S|MAF: 0.07 (G)
Location

Chromosome 10:99531546 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

HGVS name

10:g.99531546C>G

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 5 transcripts and has 2505 sample genotypes.

Variant displays