Variant: rs12109307

Variant information

Location
5:121570787
Cytogenetic region
Most severe consequence
Intergenic variant
Mapped gene(s)
Alleles
T/C/G(forward strand)
Minor allele
C
MAF
0.0675039
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 1