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rs2151532

From SNPedia

Orientationminus
Stabilizedminus
Make rs2151532(C;C)
Make rs2151532(C;T)
Make rs2151532(T;T)
ReferenceGRCh38 38.1/141
Chromosome6
Position131953590
GeneLOC100131774
is asnp
is mentioned by
dbSNPrs2151532
dbSNP (classic)rs2151532
ClinGenrs2151532
ebirs2151532
HLIrs2151532
Exacrs2151532
Gnomadrs2151532
Varsomers2151532
LitVarrs2151532
Maprs2151532
PheGenIrs2151532
Biobankrs2151532
1000 genomesrs2151532
hgdprs2151532
ensemblrs2151532
geneviewrs2151532
scholarrs2151532
googlers2151532
pharmgkbrs2151532
gwascentralrs2151532
openSNPrs2151532
23andMers2151532
SNPshotrs2151532
SNPdbers2151532
MSV3drs2151532
GWAS Ctlgrs2151532
GMAF0.1543
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 19822645OA-icon.png] Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes.