Variant: rs80196932

Variant information

Location
6:117675468
Cytogenetic region
Most severe consequence
Regulatory region variant
Mapped gene(s)
Alleles
T/C(forward strand)
Minor allele
C
MAF
0.180338
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 6