RIN2, Ras and Rab interactor 2, 54453

N. diseases: 86; N. variants: 10
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs6046396
rs6046396
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0033975
Disease:
Psychotic Disorders 		G 0.800 GeneticVariation GWASDB A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. 20889312 2010
dbSNP: rs6046396
rs6046396
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0033975
Disease:
Psychotic Disorders 		0.800 GeneticVariation GWASCAT A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. 20889312 2010
dbSNP: rs6046396
rs6046396
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0004936
Disease:
Mental disorders 		G 0.800 GeneticVariation GWASDB A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. 20889312 2010
dbSNP: rs6046396
rs6046396
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0004936
Disease:
Mental disorders 		0.800 GeneticVariation GWASCAT A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. 20889312 2010
dbSNP: rs16981087
rs16981087
Entrez Id: 54453;107987276
Gene Symbol: RIN2;LOC107987276
RIN2;LOC107987276
CUI: C0202159
Disease:
Parathyroid hormone measurement 		G 0.700 GeneticVariation GWASCAT Genome-wide meta-analysis identifies novel loci associated with parathyroid hormone level. 30134803 2018
dbSNP: rs4814894
rs4814894
Entrez Id: 54453;107987276
Gene Symbol: RIN2;LOC107987276
RIN2;LOC107987276
CUI: C0678222
Disease:
Breast Carcinoma 		A 0.700 GeneticVariation GWASCAT Association analysis identifies 65 new breast cancer risk loci. 29059683 2017
dbSNP: rs181853315
rs181853315
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C3828530
Disease:
Platelet Component Distribution Width Measurement 		T 0.700 GeneticVariation GWASCAT The Allelic Landscape of Human Blood Cell Trait Variation and Links to Common Complex Disease. 27863252 2016
dbSNP: rs6081741
rs6081741
Entrez Id: 54453;107987276
Gene Symbol: RIN2;LOC107987276
RIN2;LOC107987276
CUI: C0201657
Disease:
C-reactive protein measurement 		0.700 GeneticVariation GWASDB A genome-wide association scan on the levels of markers of inflammation in Sardinians reveals associations that underpin its complex regulation. 22291609 2012
dbSNP: rs16981145
rs16981145
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C1445957
Disease:
Serum total cholesterol measurement 		0.700 GeneticVariation GWASDB A genome-wide screen for interactions reveals a new locus on 4p15 modifying the effect of waist-to-hip ratio on total cholesterol. 22028671 2011
dbSNP: rs4813376
rs4813376
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0033975
Disease:
Psychotic Disorders 		0.700 GeneticVariation GWASDB A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. 20889312 2010
dbSNP: rs4813376
rs4813376
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0004936
Disease:
Mental disorders 		0.700 GeneticVariation GWASDB A genome-wide meta-analysis identifies novel loci associated with schizophrenia and bipolar disorder. 20889312 2010
dbSNP: rs1568718508
rs1568718508
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0423110
Disease:
Downward slant of palpebral fissure 		TC 0.700 GeneticVariation CLINVAR
dbSNP: rs1568718508
rs1568718508
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C2751321
Disease:
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 		TC 0.700 GeneticVariation CLINVAR
dbSNP: rs1568718508
rs1568718508
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0162285
Disease:
Edema of eyelid 		TC 0.700 GeneticVariation CLINVAR
dbSNP: rs1568718508
rs1568718508
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C2243051
Disease:
Large head (disorder) 		TC 0.700 GeneticVariation CLINVAR
dbSNP: rs1568718508
rs1568718508
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C0019322
Disease:
Umbilical hernia 		TC 0.700 GeneticVariation CLINVAR
dbSNP: rs1568718508
rs1568718508
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C1832446
Disease:
Sparse eyebrow 		TC 0.700 GeneticVariation CLINVAR
dbSNP: rs587776915
rs587776915
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C2751321
Disease:
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 		A 0.700 CausalMutation CLINVAR
dbSNP: rs759390822
rs759390822
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C2751321
Disease:
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 		A 0.700 CausalMutation CLINVAR
dbSNP: rs759390822
rs759390822
Entrez Id: 54453
Gene Symbol: RIN2
RIN2
CUI: C2751321
Disease:
Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis 		AC 0.700 CausalMutation CLINVAR