Variant: rs10066447

Variant information

Location
5:13242862
Cytogenetic region
Most severe consequence
Intergenic variant
Mapped gene(s)
Alleles
C/T(forward strand)
Minor allele
T
MAF
0.232339
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 1