BMPER, BMP binding endothelial regulator, 168667

N. diseases: 75; N. variants: 12
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17169634
rs17169634
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0002395
Disease:
Alzheimer's Disease 		0.800 GeneticVariation GWASDB ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. 24770881 2014
dbSNP: rs17169634
rs17169634
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0002395
Disease:
Alzheimer's Disease 		0.800 GeneticVariation GWASCAT ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. 24770881 2014
dbSNP: rs387906993
rs387906993
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C1842691
Disease:
Diaphanospondylodysostosis 		0.800 GeneticVariation UNIPROT BMPER mutation in diaphanospondylodysostosis identified by ancestral autozygosity mapping and targeted high-throughput sequencing. 20869035 2010
dbSNP: rs387906993
rs387906993
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C1842691
Disease:
Diaphanospondylodysostosis 		T 0.800 CausalMutation CLINVAR
dbSNP: rs1554300601
rs1554300601
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C1842691
Disease:
Diaphanospondylodysostosis 		A 0.700 GeneticVariation CLINVAR Diaphanospondylodysostosis: Refining the prenatal diagnosis of a rare skeletal disorder. 30006055 2019
dbSNP: rs6952495
rs6952495
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0042834
Disease:
Vital capacity 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs74629737
rs74629737
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0016529
Disease:
Forced expiratory volume function 		C 0.700 GeneticVariation GWASCAT A genome-wide association study identifies risk loci for spirometric measures among smokers of European and African ancestry. 26634245 2015
dbSNP: rs74495807
rs74495807
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0002395
Disease:
Alzheimer's Disease 		0.700 GeneticVariation GWASDB ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. 24770881 2014
dbSNP: rs74651988
rs74651988
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0002395
Disease:
Alzheimer's Disease 		0.700 GeneticVariation GWASDB ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. 24770881 2014
dbSNP: rs75353220
rs75353220
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0002395
Disease:
Alzheimer's Disease 		0.700 GeneticVariation GWASDB ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. 24770881 2014
dbSNP: rs75733828
rs75733828
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0002395
Disease:
Alzheimer's Disease 		0.700 GeneticVariation GWASDB ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. 24770881 2014
dbSNP: rs79312206
rs79312206
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C0002395
Disease:
Alzheimer's Disease 		0.700 GeneticVariation GWASDB ABCC9 gene polymorphism is associated with hippocampal sclerosis of aging pathology. 24770881 2014
dbSNP: rs1554300601
rs1554300601
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C1842691
Disease:
Diaphanospondylodysostosis 		A 0.700 CausalMutation CLINVAR
dbSNP: rs387906992
rs387906992
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C1842691
Disease:
Diaphanospondylodysostosis 		T 0.700 CausalMutation CLINVAR
dbSNP: rs387906994
rs387906994
Entrez Id: 168667
Gene Symbol: BMPER
BMPER
CUI: C1842691
Disease:
Diaphanospondylodysostosis 		A 0.700 CausalMutation CLINVAR