Variant: rs579383

Variant information

Location
11:61769111
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
G/A/T(forward strand)
Minor allele
G
MAF
0.274922
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 2