Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121912632
rs121912632
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0432228
Disease:
Brachyolmia
0.010 GeneticVariation BEFREE TRPV4 expresses in bone cell lineages and TRPV4-R616Q mutant causing Brachyolmia in human reveals "loss-of-interaction" with cholesterol. 31387748 2019
dbSNP: rs387906905
rs387906905
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0751335
Disease:
Scapuloperoneal Form of Spinal Muscular Atrophy
0.010 GeneticVariation BEFREE We report the first Italian family with SPSMA, harboring the c.806G>A mutation in TRPV4 gene (p. R269H). 26948711 2017
dbSNP: rs77975504
rs77975504
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0231557
Disease:
Abnormal bone formation
0.010 GeneticVariation BEFREE SMD Kozlowski type caused by p.Arg594His substitution in TRPV4 reveals abnormal ossification and notochordal remnants in discs and vertebrae. 28687525 2017
dbSNP: rs10735104
rs10735104
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0028754
Disease:
Obesity
0.010 GeneticVariation BEFREE Obesity as defined according to both the Asian and National Institutes of Health (NIH) criteria was significantly associated with rs10735104 (P = 0.003 and P = 0.037, respectively) in a dominant model. 25647731 2015
dbSNP: rs121912633
rs121912633
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0432228
Disease:
Brachyolmia
0.010 GeneticVariation BEFREE We generated a mouse model of the TRPV4(V620I) mutation, and found significant skeletal deformities (e.g., shortening of tibiae and digits, similar to the human disease brachyolmia) and increases in Fst/TRPV4 mRNA levels (2.8-fold). 24577120 2014
dbSNP: rs121912633
rs121912633
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C1720983
Disease:
Channelopathies
0.010 GeneticVariation BEFREE The human TRPV4(V620I) channelopathy mutation was transfected into primary porcine chondrocytes and caused significant (2.6-fold) up-regulation of follistatin (FST) expression levels. 24577120 2014
dbSNP: rs387906904
rs387906904
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0393541
Disease:
Distal Spinal Muscular Atrophy
0.010 GeneticVariation BEFREE In another child with congenital dSMA, in this case associated with bone abnormalities, we detected a previously reported mutation (p.R232C). 22526352 2012
dbSNP: rs876661124
rs876661124
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0042928
Disease:
Vocal Cord Paralysis
0.010 GeneticVariation BEFREE In a girl with dSMA and vocal cord paralysis, we detected a new variant (p.P97R) localized in the cytosolic N-terminus of the TRPV4 protein, upstream of the ankyrin-repeat domain, where the great majority of disease-associated mutations reside. 22526352 2012
dbSNP: rs876661124
rs876661124
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0393541
Disease:
Distal Spinal Muscular Atrophy
0.010 GeneticVariation BEFREE In a girl with dSMA and vocal cord paralysis, we detected a new variant (p.P97R) localized in the cytosolic N-terminus of the TRPV4 protein, upstream of the ankyrin-repeat domain, where the great majority of disease-associated mutations reside. 22526352 2012
dbSNP: rs121912633
rs121912633
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0043144
Disease:
Wheezing
0.010 GeneticVariation BEFREE Although none of the SNPs modified the risk of suffering from asthma, carriers of the TRPV1-I585V genetic variant showed a lower risk of current wheezing (odds ratio = 0.51; p = 0.01), a characteristic of active asthma, or cough (odds ratio = 0.57; p = 0.02). 20639579 2010
dbSNP: rs121912633
rs121912633
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE We now report on the association of two functional SNPs, TRPV1-I585V and TRPV4-P19S, with childhood asthma. 20639579 2010
dbSNP: rs121912633
rs121912633
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0010200
Disease:
Coughing
0.010 GeneticVariation BEFREE Although none of the SNPs modified the risk of suffering from asthma, carriers of the TRPV1-I585V genetic variant showed a lower risk of current wheezing (odds ratio = 0.51; p = 0.01), a characteristic of active asthma, or cough (odds ratio = 0.57; p = 0.02). 20639579 2010
dbSNP: rs121912633
rs121912633
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE Although none of the SNPs modified the risk of suffering from asthma, carriers of the TRPV1-I585V genetic variant showed a lower risk of current wheezing (odds ratio = 0.51; p = 0.01), a characteristic of active asthma, or cough (odds ratio = 0.57; p = 0.02). 20639579 2010
dbSNP: rs3742030
rs3742030
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0043144
Disease:
Wheezing
0.010 GeneticVariation BEFREE On the other hand, TRPV4-P19S, despite its loss-of-channel function, showed no significant association with asthma or the presence of wheezing. 20639579 2010
dbSNP: rs3742030
rs3742030
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0004096
Disease:
Asthma
0.010 GeneticVariation BEFREE On the other hand, TRPV4-P19S, despite its loss-of-channel function, showed no significant association with asthma or the presence of wheezing. 20639579 2010
dbSNP: rs3742030
rs3742030
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0264408
Disease:
Childhood asthma
0.010 GeneticVariation BEFREE We now report on the association of two functional SNPs, TRPV1-I585V and TRPV4-P19S, with childhood asthma. 20639579 2010
dbSNP: rs3742030
rs3742030
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0020625
Disease:
Hyponatremia
0.010 GeneticVariation BEFREE We show that this polymorphism is significantly associated with serum sodium concentration and with hyponatremia (serum sodium concentration < or =135 mEq/L) in 2 non-Hispanic Caucasian male populations; in addition, mean serum sodium concentration is lower among subjects with the TRPV4(P19S) allele relative to the wild-type allele. 19666518 2009
dbSNP: rs10850813
rs10850813
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0017654
Disease:
Glomerular Filtration Rate
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs7971845
rs7971845
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0201976
Disease:
Creatinine measurement, serum (procedure)
0.700 GeneticVariation GWASCAT Genetic analysis of quantitative traits in the Japanese population links cell types to complex human diseases. 29403010 2018
dbSNP: rs1555205335
rs1555205335
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0000772
Disease:
Multiple congenital anomalies
C 0.700 CausalMutation CLINVAR Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathy. 28898540 2017
dbSNP: rs1555208063
rs1555208063
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0432072
Disease:
Dysmorphic features
G 0.700 GeneticVariation CLINVAR Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathy. 28898540 2017
dbSNP: rs267607144
rs267607144
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0000772
Disease:
Multiple congenital anomalies
T 0.700 CausalMutation CLINVAR Compound heterozygous TRPV4 mutations in two siblings with a complex phenotype including severe intellectual disability and neuropathy. 28898540 2017
dbSNP: rs1555205335
rs1555205335
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0000772
Disease:
Multiple congenital anomalies
C 0.700 CausalMutation CLINVAR Gain-of-function mutation in TRPV4 identified in patients with osteonecrosis of the femoral head. 27330106 2016
dbSNP: rs1555208063
rs1555208063
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0432072
Disease:
Dysmorphic features
G 0.700 GeneticVariation CLINVAR Gain-of-function mutation in TRPV4 identified in patients with osteonecrosis of the femoral head. 27330106 2016
dbSNP: rs267607144
rs267607144
Entrez Id: 59341
Gene Symbol: TRPV4
TRPV4
CUI: C0000772
Disease:
Multiple congenital anomalies
T 0.700 CausalMutation CLINVAR Gain-of-function mutation in TRPV4 identified in patients with osteonecrosis of the femoral head. 27330106 2016