Variant: rs7706662

  1. GWAS
  2. Variants
  3. rs7706662

Variant information

Location
5:123419868
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
C/G/T(forward strand)
Minor allele
T
MAF
0.453493
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations