SPRY4-AS1, SPRY4 antisense RNA 1, 101926941

N. diseases: 18; N. variants: 23
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs10065321
rs10065321
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs10477176
rs10477176
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. 30578418 2019
dbSNP: rs153662
rs153662
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs2070715
rs2070715
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C1836233
Disease:
AIDS, PROGRESSION TO 		C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs2070715
rs2070715
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C0376705
Disease:
Viral Load result 		C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs2070715
rs2070715
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C1836232
Disease:
ACQUIRED IMMUNODEFICIENCY SYNDROME, PROGRESSION TO 		C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs2070715
rs2070715
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C1836231
Disease:
HIV-1, RESISTANCE TO 		C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs2070715
rs2070715
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C1836230
Disease:
HUMAN IMMUNODEFICIENCY VIRUS TYPE 1, SUSCEPTIBILITY TO 		C 0.700 GeneticVariation GWASCAT Association Between Single-Nucleotide Polymorphisms in HLA Alleles and Human Immunodeficiency Virus Type 1 Viral Load in Demographically Diverse, Antiretroviral Therapy-Naive Participants From the Strategic Timing of AntiRetroviral Treatment Trial. 31219150 2019
dbSNP: rs250100
rs250100
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs253443
rs253443
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0427460
Disease:
Red cell distribution width determination 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs253443
rs253443
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C1304746
Disease:
RDW - Red blood cell distribution width result 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34000
rs34000
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C0205682
Disease:
Waist-Hip Ratio 		T 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: rs34000
rs34000
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C0205682
Disease:
Waist-Hip Ratio 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs34427173
rs34427173
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Characterizing rare and low-frequency height-associated variants in the Japanese population. 31562340 2019
dbSNP: rs76271629
rs76271629
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0871470
Disease:
Systolic Pressure 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs1650911
rs1650911
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0871470
Disease:
Systolic Pressure 		G 0.700 GeneticVariation GWASCAT Genetic analysis of over 1 million people identifies 535 new loci associated with blood pressure traits. 30224653 2018
dbSNP: rs249756
rs249756
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		A 0.700 GeneticVariation GWASCAT Genetics of blood lipids among ~300,000 multi-ethnic participants of the Million Veteran Program. 30275531 2018
dbSNP: rs249767
rs249767
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C1720164
Disease:
Central corneal thickness 		T 0.700 GeneticVariation GWASCAT Cross-ancestry genome-wide association analysis of corneal thickness strengthens link between complex and Mendelian eye diseases. 29760442 2018
dbSNP: rs3853476
rs3853476
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0871470
Disease:
Systolic Pressure 		A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs3853476
rs3853476
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0428886
Disease:
Mean blood pressure 		A 0.700 GeneticVariation GWASCAT Interethnic analyses of blood pressure loci in populations of East Asian and European descent. 30487518 2018
dbSNP: rs4244029
rs4244029
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0202117
Disease:
Low density lipoprotein cholesterol measurement 		C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs4244029
rs4244029
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C1445957
Disease:
Serum total cholesterol measurement 		C 0.700 GeneticVariation GWASCAT A large electronic-health-record-based genome-wide study of serum lipids. 29507422 2018
dbSNP: rs152528
rs152528
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C1383860
Disease:
Cardiac Hypertrophy 		0.700 GeneticVariation GWASDB Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951 2011
dbSNP: rs152528
rs152528
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C0018800
Disease:
Cardiomegaly 		0.700 GeneticVariation GWASCAT Hypertrophy-associated polymorphisms ascertained in a founder cohort applied to heart failure risk and mortality. 21348951 2011
dbSNP: rs959662
rs959662
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0855197
Disease:
Malignant Testicular Germ Cell Tumor 		0.700 GeneticVariation GWASDB Variants near DMRT1, TERT and ATF7IP are associated with testicular germ cell cancer. 20543847 2010