RBM12, RNA binding motif protein 12, 10137

N. diseases: 17; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17426738
rs17426738
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs17426738
rs17426738
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs17427233
rs17427233
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs17427233
rs17427233
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6058292
rs6058292
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6058292
rs6058292
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6060536
rs6060536
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6060536
rs6060536
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6060540
rs6060540
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6060540
rs6060540
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6060545
rs6060545
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6060545
rs6060545
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6119636
rs6119636
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6119636
rs6119636
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6121019
rs6121019
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6121019
rs6121019
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6121021
rs6121021
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C1168438
Disease:
Protein C antigen measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs6121021
rs6121021
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0919677
Disease:
Protein C measurement 		0.700 GeneticVariation GWASDB Genome-wide association study identifies novel loci for plasma levels of protein C: the ARIC study. 20802025 2010
dbSNP: rs1262969313
rs1262969313
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C4539944
Disease:
SCHIZOPHRENIA 19 		C 0.700 CausalMutation CLINVAR
dbSNP: rs781720548
rs781720548
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C4539944
Disease:
SCHIZOPHRENIA 19 		A 0.700 CausalMutation CLINVAR
dbSNP: rs781720548
rs781720548
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0349204
Disease:
Nonorganic psychosis 		0.010 GeneticVariation BEFREE We replicated the association in a Finnish family in which a second RBM12 truncating mutation (c.2532delT) segregates with psychosis (P = 0.020). c.2377G>T is not fully penetrant for psychosis; however, we found that carriers unaffected by psychosis resemble patients with schizophrenia in their non-psychotic psychiatric disorder and neuropsychological test profile (P = 0.0043) as well as in their life outcomes (including an increased chance of receiving disability benefits, P = 0.011). 28628109 2017
dbSNP: rs781720548
rs781720548
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0033975
Disease:
Psychotic Disorders 		0.010 GeneticVariation BEFREE We replicated the association in a Finnish family in which a second RBM12 truncating mutation (c.2532delT) segregates with psychosis (P = 0.020). c.2377G>T is not fully penetrant for psychosis; however, we found that carriers unaffected by psychosis resemble patients with schizophrenia in their non-psychotic psychiatric disorder and neuropsychological test profile (P = 0.0043) as well as in their life outcomes (including an increased chance of receiving disability benefits, P = 0.011). 28628109 2017
dbSNP: rs781720548
rs781720548
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0036341
Disease:
Schizophrenia 		0.010 GeneticVariation BEFREE We replicated the association in a Finnish family in which a second RBM12 truncating mutation (c.2532delT) segregates with psychosis (P = 0.020). c.2377G>T is not fully penetrant for psychosis; however, we found that carriers unaffected by psychosis resemble patients with schizophrenia in their non-psychotic psychiatric disorder and neuropsychological test profile (P = 0.0043) as well as in their life outcomes (including an increased chance of receiving disability benefits, P = 0.011). 28628109 2017
dbSNP: rs781720548
rs781720548
Entrez Id: 8904;10137
Gene Symbol: CPNE1;RBM12
CPNE1;RBM12
CUI: C0004936
Disease:
Mental disorders 		0.010 GeneticVariation BEFREE We replicated the association in a Finnish family in which a second RBM12 truncating mutation (c.2532delT) segregates with psychosis (P = 0.020). c.2377G>T is not fully penetrant for psychosis; however, we found that carriers unaffected by psychosis resemble patients with schizophrenia in their non-psychotic psychiatric disorder and neuropsychological test profile (P = 0.0043) as well as in their life outcomes (including an increased chance of receiving disability benefits, P = 0.011). 28628109 2017