TCTEX1D2, Tctex1 domain containing 2, 255758

N. diseases: 19; N. variants: 1
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs886039815
rs886039815
Entrez Id: 255758
Gene Symbol: TCTEX1D2
TCTEX1D2
CUI: C0600031
Disease:
Congenital absence of spleen 		A 0.700 CausalMutation CLINVAR
dbSNP: rs886039815
rs886039815
Entrez Id: 255758
Gene Symbol: TCTEX1D2
TCTEX1D2
CUI: C0426817
Disease:
Short ribs 		A 0.700 CausalMutation CLINVAR
dbSNP: rs886039815
rs886039815
Entrez Id: 255758
Gene Symbol: TCTEX1D2
TCTEX1D2
CUI: C4551856
Disease:
Asphyxiating Thoracic Dystrophy 1 		A 0.700 CausalMutation CLINVAR
dbSNP: rs886039815
rs886039815
Entrez Id: 255758
Gene Symbol: TCTEX1D2
TCTEX1D2
CUI: C0521622
Disease:
Bilateral hydronephrosis 		A 0.700 CausalMutation CLINVAR
dbSNP: rs886039815
rs886039815
Entrez Id: 255758
Gene Symbol: TCTEX1D2
TCTEX1D2
CUI: C0175707
Disease:
Asplenia Syndrome 		A 0.700 CausalMutation CLINVAR