Variant: rs174532

Variant information

Location
11:61781402
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
G/A(forward strand)
Minor allele
A
MAF
0.100863
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 53