Variant: rs116472104

Variant information

Location
22:43486346
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
C/A(forward strand)
Minor allele
A
MAF
0.0221743
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 1