NFIB, nuclear factor I B, 4781

N. diseases: 5; N. variants: 21
Source: CURATED ×
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1554709654
rs1554709654
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		G 0.800 GeneticVariation CLINVAR NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. 30388402 2018
dbSNP: rs1554709654
rs1554709654
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		0.800 GeneticVariation UNIPROT NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. 30388402 2018
dbSNP: rs1554709662
rs1554709662
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		C 0.800 GeneticVariation CLINVAR NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. 30388402 2018
dbSNP: rs1554709662
rs1554709662
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		0.800 GeneticVariation UNIPROT NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. 30388402 2018
dbSNP: rs1554709683
rs1554709683
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		0.800 GeneticVariation UNIPROT NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. 30388402 2018
dbSNP: rs59677118
rs59677118
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0001948
Disease:
Alcohol consumption 		0.800 GeneticVariation GWASDB A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. 23743675 2013
dbSNP: rs59677118
rs59677118
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0001948
Disease:
Alcohol consumption 		0.800 GeneticVariation GWASCAT A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks. 23743675 2013
dbSNP: rs1554709654
rs1554709654
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		G 0.800 CausalMutation CLINVAR
dbSNP: rs1554709662
rs1554709662
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		C 0.800 CausalMutation CLINVAR
dbSNP: rs1554709683
rs1554709683
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		G 0.800 CausalMutation CLINVAR
dbSNP: rs7034162
rs7034162
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0029463
Disease:
Osteosarcoma 		A 0.720 GeneticVariation GWASCAT These data suggest that germline genetic variation at rs7034162 is important in osteosarcoma metastasis and that NFIB is an osteosarcoma metastasis susceptibility gene. 26084801 2015
dbSNP: rs10046853
rs10046853
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10810098
rs10810098
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0023508
Disease:
White Blood Cell Count procedure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10961430
rs10961430
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0036341
Disease:
Schizophrenia 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs10961430
rs10961430
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0021704
Disease:
Intelligence 		0.700 GeneticVariation GWASCAT Pleiotropic Meta-Analysis of Cognition, Education, and Schizophrenia Differentiates Roles of Early Neurodevelopmental and Adult Synaptic Pathways. 31374203 2019
dbSNP: rs1322985
rs1322985
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0014772
Disease:
Red Blood Cell Count measurement 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs424539
rs424539
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C1305855
Disease:
Body mass index 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs7031064
rs7031064
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C1305855
Disease:
Body mass index 		A 0.700 GeneticVariation GWASCAT Meta-analysis of genome-wide association studies for body fat distribution in 694 649 individuals of European ancestry. 30239722 2019
dbSNP: rs72700531
rs72700531
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0869220
Disease:
Adverse effects, not elsewhere classified 		T 0.700 GeneticVariation GWASCAT Genetic variation in the Estonian population: pharmacogenomics study of adverse drug effects using electronic health records. 30420678 2019
dbSNP: rs10810107
rs10810107
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0596887
Disease:
mathematical ability 		C 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: rs1328006
rs1328006
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
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: rs1554709792
rs1554709792
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		A 0.700 CausalMutation CLINVAR NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. 30388402 2018
dbSNP: rs4237133
rs4237133
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C0596887
Disease:
mathematical ability 		C 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: rs72702916
rs72702916
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4280669
Disease:
Velopharyngeal dysfunction 		0.700 GeneticVariation GWASCAT GWAS reveals loci associated with velopharyngeal dysfunction. 29855589 2018
dbSNP: rs764333096
rs764333096
Entrez Id: 4781
Gene Symbol: NFIB
NFIB
CUI: C4748993
Disease:
MACROCEPHALY, ACQUIRED, WITH IMPAIRED INTELLECTUAL DEVELOPMENT 		A 0.700 GeneticVariation CLINVAR NFIB Haploinsufficiency Is Associated with Intellectual Disability and Macrocephaly. 30388402 2018