Variant: rs2116830

Variant information

Location
10:76886778
Cytogenetic region
Most severe consequence
3 prime utr variant
Mapped gene(s)
Alleles
G/T(forward strand)
Minor allele
T
MAF
0.0704474
GWAS Catalog data is currently mapped to Genome Assembly GRCh38.p14 and dbSNP Build156
Available data:

Associations 1