Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1305542291
rs1305542291
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4748658
Disease:
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA 		T 0.800 CausalMutation CLINVAR
dbSNP: rs1305542291
rs1305542291
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4748658
Disease:
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA 		0.800 GeneticVariation UNIPROT
dbSNP: rs1239725461
rs1239725461
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4748658
Disease:
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1239725461
rs1239725461
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4072872
Disease:
obsolete Rod-cone dystrophy 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1239725461
rs1239725461
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0392557
Disease:
Nuclear cataract 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1239725461
rs1239725461
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0026106
Disease:
Mild Mental Retardation 		A 0.700 GeneticVariation CLINVAR
dbSNP: rs1305542291
rs1305542291
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0026351
Disease:
Moderate intellectual disability 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1305542291
rs1305542291
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4072872
Disease:
obsolete Rod-cone dystrophy 		T 0.700 GeneticVariation CLINVAR
dbSNP: rs1395475624
rs1395475624
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4072872
Disease:
obsolete Rod-cone dystrophy 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1395475624
rs1395475624
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0026351
Disease:
Moderate intellectual disability 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs1395475624
rs1395475624
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4748658
Disease:
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA 		G 0.700 CausalMutation CLINVAR
dbSNP: rs1555447569
rs1555447569
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4748658
Disease:
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA 		C 0.700 CausalMutation CLINVAR
dbSNP: rs1555558169
rs1555558169
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C4748658
Disease:
INTELLECTUAL DEVELOPMENTAL DISORDER AND RETINITIS PIGMENTOSA 		C 0.700 CausalMutation CLINVAR
dbSNP: rs10851889
rs10851889
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs10851889
rs10851889
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11072617
rs11072617
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11072625
rs11072625
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs1116535
rs1116535
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11632765
rs11632765
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs11633869
rs11633869
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		C 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12440511
rs12440511
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12904417
rs12904417
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs12912475
rs12912475
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		T 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs16968467
rs16968467
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		G 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017
dbSNP: rs17464903
rs17464903
Entrez Id: 49855
Gene Symbol: SCAPER
SCAPER
CUI: C0023467
Disease:
Leukemia, Myelocytic, Acute 		A 0.700 GeneticVariation GWASCAT Genome-wide haplotype association study identify the FGFR2 gene as a risk gene for acute myeloid leukemia. 27903959 2017