Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs875989883
rs875989883
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.800 GeneticVariation CLINVAR

dbSNP: rs875989883
rs875989883
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		C 0.800 CausalMutation CLINVAR

dbSNP: rs1556206403
rs1556206403
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		C 0.800 CausalMutation CLINVAR

dbSNP: rs1556200989
rs1556200989
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.800 CausalMutation CLINVAR

dbSNP: rs1556135308
rs1556135308
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.800 CausalMutation CLINVAR

dbSNP: rs1556091855
rs1556091855
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		C 0.800 CausalMutation CLINVAR

dbSNP: rs1556014287
rs1556014287
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		C 0.800 CausalMutation CLINVAR

dbSNP: rs137853270
rs137853270
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		C 0.800 CausalMutation CLINVAR

dbSNP: rs137853269
rs137853269
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.800 CausalMutation CLINVAR

dbSNP: rs886042234
rs886042234
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.700 GeneticVariation CLINVAR

dbSNP: rs886042234
rs886042234
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886041695
rs886041695
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886041631
rs886041631
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		C 0.700 CausalMutation CLINVAR

dbSNP: rs886041374
rs886041374
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886041369
rs886041369
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886041367
rs886041367
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		ATGAT 0.700 CausalMutation CLINVAR

dbSNP: rs886041364
rs886041364
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		ATGAT 0.700 CausalMutation CLINVAR

dbSNP: rs886041363
rs886041363
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886041361
rs886041361
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886041359
rs886041359
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886041296
rs886041296
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.700 CausalMutation CLINVAR

dbSNP: rs886041227
rs886041227
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886041226
rs886041226
PHEX ; PTCHD1-AS
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		T 0.700 CausalMutation CLINVAR

dbSNP: rs886041225
rs886041225
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		A 0.700 CausalMutation CLINVAR

dbSNP: rs866429868
rs866429868
PHEX
CUI: C0733682
Disease: Hypophosphatemic Rickets, X-Linked Dominant
Hypophosphatemic Rickets, X-Linked Dominant 		T 0.700 CausalMutation CLINVAR