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rs9402373

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs9402373(C;G)
Make rs9402373(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position131956291
GeneLOC100131774
is asnp
is mentioned by
dbSNPrs9402373
ebirs9402373
HLIrs9402373
Exacrs9402373
Varsomers9402373
Maprs9402373
PheGenIrs9402373
hapmaprs9402373
1000 genomesrs9402373
hgdprs9402373
ensemblrs9402373
gopubmedrs9402373
geneviewrs9402373
scholarrs9402373
googlers9402373
pharmgkbrs9402373
gwascentralrs9402373
openSNPrs9402373
23andMers9402373
23andMe allrs9402373
SNP Nexus

SNPshotrs9402373
SNPdbers9402373
MSV3drs9402373
GWAS Ctlgrs9402373
GMAF0.242
Max Magnitude0
? (C;C) (C;G) (G;G) 28
[PMID 19822645OA-icon.png] Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with Schistosomes
OMIM121009
DescCONNECTIVE TISSUE GROWTH FACTOR; CTGF
Variant
Relatedalso
OMIM604201
Desc
Variant
Relatedalso


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