Variant: rs3212335

  1. GWAS
  2. Variants
  3. rs3212335

Variant information

Location
15:26766994
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
C/A/G/T(forward strand)
Minor allele
T
MAF
0.317896
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations