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rs1256196

From SNPedia

Orientationplus
Stabilizedplus
Make rs1256196(A;A)
Make rs1256196(A;T)
Make rs1256196(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position122641075
is asnp
is mentioned by
dbSNPrs1256196
ebirs1256196
HLIrs1256196
Exacrs1256196
Varsomers1256196
Maprs1256196
PheGenIrs1256196
hapmaprs1256196
1000 genomesrs1256196
hgdprs1256196
ensemblrs1256196
gopubmedrs1256196
geneviewrs1256196
scholarrs1256196
googlers1256196
pharmgkbrs1256196
gwascentralrs1256196
openSNPrs1256196
23andMers1256196
23andMe allrs1256196
SNP Nexus

SNPshotrs1256196
SNPdbers1256196
MSV3drs1256196
GWAS Ctlgrs1256196
GMAF0.3035
Max Magnitude
? (A;A) (A;T) (T;T) 28
OMIM121009
DescCONNECTIVE TISSUE GROWTH FACTOR; CTGF
Variant
Relatedalso
OMIM604201
Desc
Variant
Relatedalso
[PMID 19822645OA-icon.png] Variants of CTGF are associated with hepatic fibrosis in Chinese, Sudanese, and Brazilians infected with schistosomes.