Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121918499
rs121918499
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		G 0.840 CausalMutation CLINVAR

dbSNP: rs121918499
rs121918499
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		A 0.840 CausalMutation CLINVAR

dbSNP: rs776587763
rs776587763
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		A 0.820 CausalMutation CLINVAR

dbSNP: rs121918502
rs121918502
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.820 CausalMutation CLINVAR

dbSNP: rs121918488
rs121918488
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		T 0.820 CausalMutation CLINVAR

dbSNP: rs121918488
rs121918488
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.820 CausalMutation CLINVAR

dbSNP: rs121918510
rs121918510
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		G 0.810 CausalMutation CLINVAR

dbSNP: rs121918487
rs121918487
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		T 0.810 CausalMutation CLINVAR

dbSNP: rs121918506
rs121918506
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		G 0.800 CausalMutation CLINVAR

dbSNP: rs121918506
rs121918506
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		G 0.800 GeneticVariation CLINVAR

dbSNP: rs121918506
rs121918506
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.800 GeneticVariation CLINVAR

dbSNP: rs121918495
rs121918495
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		G 0.800 CausalMutation CLINVAR

dbSNP: rs121913478
rs121913478
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.800 CausalMutation CLINVAR

dbSNP: rs1057519047
rs1057519047
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.800 GeneticVariation CLINVAR

dbSNP: rs1057519047
rs1057519047
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		0.800 GeneticVariation UNIPROT

dbSNP: rs77543610
rs77543610
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.760 CausalMutation CLINVAR

dbSNP: rs121918497
rs121918497
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		G 0.720 CausalMutation CLINVAR

dbSNP: rs121918505
rs121918505
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		G 0.710 CausalMutation CLINVAR

dbSNP: rs886037837
rs886037837
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs879253721
rs879253721
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs879253719
rs879253719
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1554927408
rs1554927408
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		T 0.700 CausalMutation CLINVAR

dbSNP: rs1434545235
rs1434545235
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		C 0.700 CausalMutation CLINVAR

dbSNP: rs121918503
rs121918503
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		A 0.700 CausalMutation CLINVAR

dbSNP: rs121918491
rs121918491
FGFR2
CUI: C0220658
Disease: Pfeiffer Syndrome
Pfeiffer Syndrome 		T 0.700 CausalMutation CLINVAR