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rs1337791

From SNPedia

Orientationminus
Stabilizedminus
Make rs1337791(C;C)
Make rs1337791(C;T)
Make rs1337791(T;T)
ReferenceGRCh38 38.1/141
Chromosome13
Position97866334
is asnp
is mentioned by
dbSNPrs1337791
ebirs1337791
HLIrs1337791
Exacrs1337791
Varsomers1337791
Maprs1337791
PheGenIrs1337791
hapmaprs1337791
1000 genomesrs1337791
hgdprs1337791
ensemblrs1337791
gopubmedrs1337791
geneviewrs1337791
scholarrs1337791
googlers1337791
pharmgkbrs1337791
gwascentralrs1337791
openSNPrs1337791
23andMers1337791
23andMe allrs1337791
SNP Nexus

SNPshotrs1337791
SNPdbers1337791
MSV3drs1337791
GWAS Ctlgrs1337791
GMAF0.2562
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 21876774OA-icon.png] Association analysis of canonical Wnt signalling genes in diabetic nephropathy