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rs11966728

From SNPedia

Orientationplus
Stabilizedplus
Make rs11966728(C;C)
Make rs11966728(C;T)
Make rs11966728(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position131955465
GeneLOC100131774
is asnp
is mentioned by
dbSNPrs11966728
ebirs11966728
HLIrs11966728
Exacrs11966728
Varsomers11966728
Maprs11966728
PheGenIrs11966728
hapmaprs11966728
1000 genomesrs11966728
hgdprs11966728
ensemblrs11966728
gopubmedrs11966728
geneviewrs11966728
scholarrs11966728
googlers11966728
pharmgkbrs11966728
gwascentralrs11966728
openSNPrs11966728
23andMers11966728
23andMe allrs11966728
SNP Nexus

SNPshotrs11966728
SNPdbers11966728
MSV3drs11966728
GWAS Ctlgrs11966728
GMAF0.214
Max Magnitude
? (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 19822645OA-icon.png] Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes.