Variant: rs6884993

  1. GWAS
  2. Variants
  3. rs6884993

Variant information

Location
5:123410834
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
C/A/T(forward strand)
Minor allele
C
MAF
0.307496
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations