Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1131692330
rs1131692330
Entrez Id: 9319
Gene Symbol: TRIP13
TRIP13
CUI: C4539839
Disease:
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3 		C 0.700 CausalMutation CLINVAR
dbSNP: rs376882637
rs376882637
Entrez Id: 9319
Gene Symbol: TRIP13
TRIP13
CUI: C4539839
Disease:
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 3 		T 0.700 CausalMutation CLINVAR
dbSNP: rs376882637
rs376882637
Entrez Id: 9319
Gene Symbol: TRIP13
TRIP13
CUI: C0027708
Disease:
Nephroblastoma 		0.010 GeneticVariation BEFREE Our findings suggest that TRIP13 c.1060C>T mutation may be infrequent in Pakistani WT cases. 31574018 2020
dbSNP: rs376882637
rs376882637
Entrez Id: 9319
Gene Symbol: TRIP13
TRIP13
CUI: C1333015
Disease:
Childhood Kidney Wilms Tumor 		0.010 GeneticVariation BEFREE Our findings suggest that TRIP13 c.1060C>T mutation may be infrequent in Pakistani WT cases. 31574018 2020