Variant: rs7541882

Variant information

Location
1:63655898
Cytogenetic region
Most severe consequence
Intron variant
Mapped gene(s)
Alleles
A/C/T(forward strand)
Minor allele
C
MAF
0.29533
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 1