Variant: rs10195252

Variant information

Location
2:164656581
Cytogenetic region
Most severe consequence
Intergenic variant
Mapped gene(s)
Alleles
T/C(forward strand)
Minor allele
C
MAF
0.395997
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 96