Variant: rs1005464

Variant information

Location
20:6775501
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
G/A(forward strand)
Minor allele
A
MAF
0.22449
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 1