Variant: rs28817415

Variant information

Location
4:76480299
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
C/T(forward strand)
Minor allele
T
MAF
0.223116
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 18