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rs6917644

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in complete genomics
Make rs6917644(A;G)
Make rs6917644(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position131944525
GeneLOC100131774
is asnp
is mentioned by
dbSNPrs6917644
ebirs6917644
HLIrs6917644
Exacrs6917644
Varsomers6917644
Maprs6917644
PheGenIrs6917644
hapmaprs6917644
1000 genomesrs6917644
hgdprs6917644
ensemblrs6917644
gopubmedrs6917644
geneviewrs6917644
scholarrs6917644
googlers6917644
pharmgkbrs6917644
gwascentralrs6917644
openSNPrs6917644
23andMers6917644
23andMe allrs6917644
SNP Nexus

SNPshotrs6917644
SNPdbers6917644
MSV3drs6917644
GWAS Ctlgrs6917644
GMAF0.09734
Max Magnitude0
? (A;A) (A;G) (G;G) 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.