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rs9399005

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9399005(C;T)
Make rs9399005(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position131947824
GeneTBC1D2B
is asnp
is mentioned by
dbSNPrs9399005
ebirs9399005
HLIrs9399005
Exacrs9399005
Varsomers9399005
Maprs9399005
PheGenIrs9399005
hapmaprs9399005
1000 genomesrs9399005
hgdprs9399005
ensemblrs9399005
gopubmedrs9399005
geneviewrs9399005
scholarrs9399005
googlers9399005
pharmgkbrs9399005
gwascentralrs9399005
openSNPrs9399005
23andMers9399005
23andMe allrs9399005
SNP Nexus

SNPshotrs9399005
SNPdbers9399005
MSV3drs9399005
GWAS Ctlgrs9399005
GMAF0.2911
Max Magnitude0
? (C;C) (C;T) (T;T) 28

[PMID 19243500] Validation of connective tissue growth factor (CTGF/CCN2) and its gene polymorphisms as noninvasive biomarkers for the assessment of liver fibrosis


[PMID 20032097] Association Between a CTGF Gene Polymorphism and Systemic Sclerosis in a French Population


[PMID 19822645OA-icon.png] Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes.


[PMID 24121259] The Influence of CTGF Single-Nucleotide Polymorphisms on Outcomes in Crohn's Disease


[PMID 25502877OA-icon.png] Investigating the association between polymorphisms in connective tissue growth factor and susceptibility to colon carcinoma