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rs1746825

From SNPedia

Orientationplus
Stabilizedplus
Make rs1746825(C;C)
Make rs1746825(C;T)
Make rs1746825(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position107386275
is asnp
is mentioned by
dbSNPrs1746825
ClinGenrs1746825
ebirs1746825
HLIrs1746825
Exacrs1746825
Varsomers1746825
Maprs1746825
PheGenIrs1746825
hapmaprs1746825
1000 genomesrs1746825
hgdprs1746825
ensemblrs1746825
gopubmedrs1746825
geneviewrs1746825
scholarrs1746825
googlers1746825
pharmgkbrs1746825
gwascentralrs1746825
openSNPrs1746825
23andMers1746825
23andMe allrs1746825
SNP Nexus

SNPshotrs1746825
SNPdbers1746825
MSV3drs1746825
GWAS Ctlgrs1746825
GMAF0.348
Max Magnitude

[PMID 22144504OA-icon.png] Polymorphic variation in the GC and CASR genes and associations with vitamin D metabolite concentration and metachronous colorectal neoplasia