IFT43, intraflagellar transport 43, 112752

N. diseases: 84; N. variants: 28
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555360222
rs1555360222
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3553762
Disease:
LOEYS-DIETZ SYNDROME 4
T 0.700 CausalMutation CLINVAR
dbSNP: rs1555360229
rs1555360229
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3553762
Disease:
LOEYS-DIETZ SYNDROME 4
A 0.700 CausalMutation CLINVAR
dbSNP: rs1555360229
rs1555360229
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C4707243
Disease:
Familial thoracic aortic aneurysm and aortic dissection
A 0.700 GeneticVariation CLINVAR
dbSNP: rs1555361385
rs1555361385
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3810012
Disease:
RIENHOFF SYNDROME
AT 0.700 CausalMutation CLINVAR
dbSNP: rs1555369050
rs1555369050
Entrez Id: 112752;105370573
Gene Symbol: IFT43;LOC105370573
IFT43;LOC105370573
CUI: C0036996
Disease:
Short Rib-Polydactyly Syndrome
C 0.700 GeneticVariation CLINVAR
dbSNP: rs387906514
rs387906514
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C1862511
Disease:
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA, FAMILIAL, 1 (disorder)
A 0.700 CausalMutation CLINVAR
dbSNP: rs387907107
rs387907107
Entrez Id: 112752
Gene Symbol: IFT43
IFT43
CUI: C4551571
Disease:
Cranioectodermal dysplasia
G 0.700 CausalMutation CLINVAR
dbSNP: rs587777617
rs587777617
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3553762
Disease:
LOEYS-DIETZ SYNDROME 4
T 0.700 GeneticVariation CLINVAR
dbSNP: rs587777617
rs587777617
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3810012
Disease:
RIENHOFF SYNDROME
T 0.700 CausalMutation CLINVAR
dbSNP: rs767548724
rs767548724
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3810012
Disease:
RIENHOFF SYNDROME
G 0.700 GeneticVariation CLINVAR
dbSNP: rs769724508
rs769724508
Entrez Id: 112752
Gene Symbol: IFT43
IFT43
CUI: C0036996
Disease:
Short Rib-Polydactyly Syndrome
A 0.700 GeneticVariation CLINVAR
dbSNP: rs769724508
rs769724508
Entrez Id: 112752
Gene Symbol: IFT43
IFT43
CUI: C4693420
Disease:
SHORT-RIB THORACIC DYSPLASIA 18 WITH POLYDACTYLY
A 0.700 CausalMutation CLINVAR
dbSNP: rs796051885
rs796051885
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3810012
Disease:
RIENHOFF SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs875989816
rs875989816
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3810012
Disease:
RIENHOFF SYNDROME
G 0.700 CausalMutation CLINVAR
dbSNP: rs875989817
rs875989817
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C3810012
Disease:
RIENHOFF SYNDROME
A 0.700 CausalMutation CLINVAR
dbSNP: rs11621270
rs11621270
Entrez Id: 112752
Gene Symbol: IFT43
IFT43
CUI: C0025295
Disease:
Meningitis, Pneumococcal
0.010 GeneticVariation BEFREE In a prospective nationwide cohort of patients with pneumococcal meningitis, we performed a genetic association study and found that single-nucleotide polymorphisms in the inflammasome genes CARD8 (rs2043211) and NLRP1 (rs11621270) are associated with poor disease outcome. 23053059 2013
dbSNP: rs2268626
rs2268626
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C0000846
Disease:
Agenesis
0.010 GeneticVariation BEFREE To evaluate the association of the polymorphisms in the TGFB3 gene (rs2268626) and the BMP4 gene (rs17563) with isolated human tooth agenesis. 22191848 2012
dbSNP: rs3917200
rs3917200
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C0340164
Disease:
Lofgrens syndrome
0.010 GeneticVariation BEFREE SNPs in TGF-β2 (rs1891467) and TGF-β3 (rs3917200) were investigated in 296 patients with sarcoidosis (acute/self remitting, n = 70 (including 62 patients with Löfgren's syndrome); chronic, n = 168; acute/chronic, n = 58) by real-time PCR. 21148227 2011
dbSNP: rs3917200
rs3917200
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C0036202
Disease:
Sarcoidosis
0.010 GeneticVariation BEFREE Moreover, there is evidence that rs3917200 is involved in the development of lung fibrosis in sarcoidosis. 21148227 2011
dbSNP: rs3917200
rs3917200
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C0034069
Disease:
Pulmonary Fibrosis
0.010 GeneticVariation BEFREE Moreover, there is evidence that rs3917200 is involved in the development of lung </span>fibrosis</span> in sarcoidosis. 21148227 2011
dbSNP: rs11466414
rs11466414
Entrez Id: 7043;112752
Gene Symbol: TGFB3;IFT43
TGFB3;IFT43
CUI: C0852036
Disease:
Pregnancy associated hypertension
0.010 GeneticVariation BEFREE A fetal TGF-beta3 polymorphism (rs11466414) is associated with PIH in a predominantly Hispanic population. 19628198 2009