Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs848512
rs848512
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0004096
Disease:
Asthma
0.710 GeneticVariation BEFREE This study found that several new genes might be associated with total IgE in asthmatics, such as CRIM1 (rs848512, P = 1.18×10(-6); rs711254, P = 6.73×10(-6)), ZNF71 (rs10404342, P = 7.60×10(-6)), TLN1 (rs4879926, P = 7.74×10(-6)), and SYNPO2 (rs1472066, P = 8.36×10(-6); rs1038770, P = 8.66×10(-6)). 23967269 2013
dbSNP: rs848512
rs848512
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0004096
Disease:
Asthma
0.710 GeneticVariation GWASCAT This study found that several new genes might be associated with total IgE in asthmatics, such as CRIM1 (rs848512, P = 1.18×10(-6); rs711254, P = 6.73×10(-6)), ZNF71 (rs10404342, P = 7.60×10(-6)), TLN1 (rs4879926, P = 7.74×10(-6)), and SYNPO2 (rs1472066, P = 8.36×10(-6); rs1038770, P = 8.66×10(-6)). 23967269 2013
dbSNP: rs145029810
rs145029810
Entrez Id: 51232;100288911
Gene Symbol: CRIM1;CRIM1-DT
CRIM1;CRIM1-DT
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs17018786
rs17018786
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs2216099
rs2216099
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0042834
Disease:
Vital capacity
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs3821169
rs3821169
Entrez Id: 51232;100288911
Gene Symbol: CRIM1;CRIM1-DT
CRIM1;CRIM1-DT
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs848602
rs848602
Entrez Id: 9637;51232
Gene Symbol: FEZ2;CRIM1
FEZ2;CRIM1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs848602
rs848602
Entrez Id: 9637;51232
Gene Symbol: FEZ2;CRIM1
FEZ2;CRIM1
CUI: C0005890
Disease:
Body Height
0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs181698387
rs181698387
Entrez Id: 51232;100288911
Gene Symbol: CRIM1;CRIM1-DT
CRIM1;CRIM1-DT
CUI: C0596887
Disease:
mathematical ability
T 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs6708545
rs6708545
Entrez Id: 51232;100288911
Gene Symbol: CRIM1;CRIM1-DT
CRIM1;CRIM1-DT
CUI: C0596887
Disease:
mathematical ability
A 0.700 GeneticVariation GWASCAT Gene discovery and polygenic prediction from a genome-wide association study of educational attainment in 1.1 million individuals. 30038396 2018
dbSNP: rs7562790
rs7562790
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0429097
Disease:
QRS complex feature
0.700 GeneticVariation GWASCAT 52 Genetic Loci Influencing Myocardial Mass. 27659466 2016
dbSNP: rs3755206
rs3755206
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0005890
Disease:
Body Height
T 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies of adult height in East Asians identifies 17 novel loci. 25429064 2015
dbSNP: rs711245
rs711245
Entrez Id: 9637;51232
Gene Symbol: FEZ2;CRIM1
FEZ2;CRIM1
CUI: C0005890
Disease:
Body Height
A 0.700 GeneticVariation GWASCAT Defining the role of common variation in the genomic and biological architecture of adult human height. 25282103 2014
dbSNP: rs7562790
rs7562790
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0018803
Disease:
Heart Function Tests
G 0.700 GeneticVariation GWASDB Common variants in 22 loci are associated with QRS duration and cardiac ventricular conduction. 21076409 2010
dbSNP: rs113372122
rs113372122
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C4520843
Disease:
Pterygium of eye
0.010 GeneticVariation BEFREE In this study, a Northern Irish family affected by pterygium but reporting little direct exposure to UV was identified carrying a missense variant in CRIM1 NM_016441.2: c.1235 A > C (H412P) through whole-exome sequencing and subsequent analysis. 30365943 2019
dbSNP: rs113372122
rs113372122
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0033999
Disease:
Pterygium
0.010 GeneticVariation BEFREE In this study, a Northern Irish family affected by pterygium but reporting little direct exposure to UV was identified carrying a missense variant in CRIM1 NM_016441.2: c.1235 A > C (H412P) through whole-exome sequencing and subsequent analysis. 30365943 2019
dbSNP: rs113372122
rs113372122
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C1867441
Disease:
Pterygium Of Conjunctiva And Cornea
0.010 GeneticVariation BEFREE In this study, a Northern Irish family affected by pterygium but reporting little direct exposure to UV was identified carrying a missense variant in CRIM1 NM_016441.2: c.1235 A > C (H412P) through whole-exome sequencing and subsequent analysis. 30365943 2019
dbSNP: rs711254
rs711254
Entrez Id: 51232
Gene Symbol: CRIM1
CRIM1
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE This study found that several new genes might be associated with total IgE in asthmatics, such as CRIM1 (rs848512, P = 1.18×10(-6); rs711254, P = 6.73×10(-6)), ZNF71 (rs10404342, P = 7.60×10(-6)), TLN1 (rs4879926, P = 7.74×10(-6)), and SYNPO2 (rs1472066, P = 8.36×10(-6); rs1038770, P = 8.66×10(-6)). 23967269 2013