Variant: rs78646877

Variant information

Location
5:43569800
Cytogenetic region
Most severe consequence
Intergenic variant
Mapped gene(s)
Alleles
A/G(forward strand)
Minor allele
G
MAF
0.0176609
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 1