Original source

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

Alleles
T/C|Ancestral: C|Ambiguity code: Y|MAF: 0.41 (T)
Location

Chromosome 10:99531715 (forward strand)|View in location tab

Most severe consequence
 
Upstream gene variant
Evidence status

Synonyms

Archive dbSNP rs58932635

HGVS name

10:g.99531715T>C

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 5 transcripts and has 2509 sample genotypes.

Variant displays