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rs12526196

From SNPedia

Orientationplus
Stabilizedplus
Make rs12526196(C;C)
Make rs12526196(C;T)
Make rs12526196(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position131942336
GeneLOC100131774
is asnp
is mentioned by
dbSNPrs12526196
ebirs12526196
HLIrs12526196
Exacrs12526196
Varsomers12526196
Maprs12526196
PheGenIrs12526196
hapmaprs12526196
1000 genomesrs12526196
hgdprs12526196
ensemblrs12526196
gopubmedrs12526196
geneviewrs12526196
scholarrs12526196
googlers12526196
pharmgkbrs12526196
gwascentralrs12526196
openSNPrs12526196
23andMers12526196
23andMe allrs12526196
SNP Nexus

SNPshotrs12526196
SNPdbers12526196
MSV3drs12526196
GWAS Ctlgrs12526196
GMAF0.1102
Max Magnitude
? (C;C) (C;T) (T;T) 28
[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