WNT5A, Wnt family member 5A, 7474

N. diseases: 375; N. variants: 11
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs387906663
rs387906663
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		0.800 GeneticVariation UNIPROT WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
dbSNP: rs786200925
rs786200925
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		0.800 GeneticVariation UNIPROT WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
dbSNP: rs387906663
rs387906663
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		G 0.800 CausalMutation CLINVAR
dbSNP: rs786200925
rs786200925
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		G 0.800 CausalMutation CLINVAR
dbSNP: rs815540
rs815540
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0005890
Disease:
Body Height 		0.700 GeneticVariation GWASCAT Leveraging Polygenic Functional Enrichment to Improve GWAS Power. 30595370 2019
dbSNP: rs786204836
rs786204836
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0265205
Disease:
Robinow Syndrome 		C 0.700 CausalMutation CLINVAR De novo WNT5A-associated autosomal dominant Robinow syndrome suggests specificity of genotype and phenotype. 24716670 2015
dbSNP: rs786200925
rs786200925
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0265205
Disease:
Robinow Syndrome 		G 0.700 CausalMutation CLINVAR WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
dbSNP: rs869312850
rs869312850
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0265205
Disease:
Robinow Syndrome 		G 0.700 CausalMutation CLINVAR WNT5A mutations in patients with autosomal dominant Robinow syndrome. 19918918 2010
dbSNP: rs1553677967
rs1553677967
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		TGCAGCC 0.700 GeneticVariation CLINVAR
dbSNP: rs1553677971
rs1553677971
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		C 0.700 GeneticVariation CLINVAR
dbSNP: rs587784562
rs587784562
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		G 0.700 GeneticVariation CLINVAR
dbSNP: rs786204836
rs786204836
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C4551475
Disease:
ROBINOW SYNDROME, AUTOSOMAL DOMINANT 1 		C 0.700 CausalMutation CLINVAR
dbSNP: rs504849
rs504849
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0000768
Disease:
Congenital Abnormality 		0.010 GeneticVariation BEFREE Individuals carrying a homozygous genotype CC (rs524153) or GG (rs504849) had a similarly reduced risk of conotruncal malformations. 26278011 2015
dbSNP: rs524153
rs524153
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0000768
Disease:
Congenital Abnormality 		0.010 GeneticVariation BEFREE Individuals carrying a homozygous genotype CC (rs524153) or GG (rs504849) had a similarly reduced risk of conotruncal malformations. 26278011 2015
dbSNP: rs1439009595
rs1439009595
Entrez Id: 7474
Gene Symbol: WNT5A
WNT5A
CUI: C0002736
Disease:
Amyotrophic Lateral Sclerosis 		0.010 GeneticVariation BEFREE Changes in Wnt5a and Fzd2 expression in the spinal cord of SOD1(G9</span>3A) transgenic mice (ALS), SOD1(G93A) transfected NSC-34 cells, and primary cultures of astrocytes from SOD1(G93A) transgenic mice were detected by immunofluorescent staining, reverse transcription-polymerase chain reaction (RT-PCR) and Western blotting. 23826406 2013