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: rs152524
rs152524
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C0020538
Disease:
Hypertensive disease
0.010 GeneticVariation BEFREE Single and multilocus family-based analysis revealed that genetic variation within FGF1 haploblock 1 was associated with hypertension and identified a common intronic single nucleotide polymorphism, rs152524, as the major driver of this association (P=0.0026). 17909102 2007
dbSNP: rs17098760
rs17098760
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0027404
Disease:
Narcolepsy
0.700 GeneticVariation GWASDB Genome-wide association database developed in the Japanese Integrated Database Project. 19629137 2009
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
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: rs250108
rs250108
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C4733092
Disease:
estrogen receptor-negative breast cancer
0.010 GeneticVariation BEFREE In contrast, FGF1 rs250108 was significantly associated with the risk of ER-negative breast cancer (OR (95% CI) = 1.68 (1.20-2.35) for CT + TT vs. CC genotype) but not ER-positive breast cancer. 23143756 2013
dbSNP: rs250108
rs250108
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C2938924
Disease:
Oestrogen receptor positive breast cancer
0.010 GeneticVariation BEFREE Our findings show a suggestively stronger association between FGFR2 rs2981582 and ER-positive breast cancer risk and suggest a greater association of FGF1 rs250108 and RBFOX2 rs2051579 with ER-negative compared to ER-positive breast cancer. 23143756 2013
dbSNP: rs451275
rs451275
Entrez Id: 101926941
Gene Symbol: SPRY4-AS1
SPRY4-AS1
CUI: C0038436
Disease:
Post-Traumatic Stress Disorder
0.010 GeneticVariation BEFREE Haplotype analysis revealed that the C/G haplotype (rs451275/rs386231) was significantly associated with PTSD (p=0.001). 23146198 2013
dbSNP: rs7727832
rs7727832
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C4721610
Disease:
Carcinoma, Ovarian Epithelial
0.010 GeneticVariation BEFREE In particular, FGF1 [fibroblast growth factor 1 (acidic)] SNP rs7727832 showed the most significant association with ovarian cancer (odds ratio, 2.27; 95% CI, 1.31-3.95). 24146310 2014
dbSNP: rs7727832
rs7727832
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C1140680
Disease:
Malignant neoplasm of ovary
0.010 GeneticVariation BEFREE In particular, FGF1 [fibroblast growth factor 1 (acidic)] SNP rs7727832 showed the most significant association with ovarian cancer (odds ratio, 2.27; 95% CI, 1.31-3.95). 24146310 2014
dbSNP: rs7727832
rs7727832
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C0919267
Disease:
ovarian neoplasm
0.010 GeneticVariation BEFREE In particular, FGF1 [fibroblast growth factor 1 (acidic)] SNP rs7727832 showed the most significant association with ovarian cancer (odds ratio, 2.27; 95% CI, 1.31-3.95). 24146310 2014
dbSNP: rs34011
rs34011
Entrez Id: 2246;101926941
Gene Symbol: FGF1;SPRY4-AS1
FGF1;SPRY4-AS1
CUI: C0002395
Disease:
Alzheimer's Disease
0.010 GeneticVariation BEFREE We found that the genotype distribution of rs34011 was significantly different between AD and control group (χ(2) = 9.048, df = 2, P = 0.011). 24464990 2014
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: 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: 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: 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: 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: 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: 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: 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: 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: 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