FGF23, fibroblast growth factor 23, 8074

N. diseases: 305; N. variants: 19
Disease: TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104894342
rs104894342
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A new missense mutation in FGF23 gene in a male with hyperostosis-hyperphosphatemia syndrome (HHS). 24680727 2014
dbSNP: rs104894343
rs104894343
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A new missense mutation in FGF23 gene in a male with hyperostosis-hyperphosphatemia syndrome (HHS). 24680727 2014
dbSNP: rs104894344
rs104894344
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A new missense mutation in FGF23 gene in a male with hyperostosis-hyperphosphatemia syndrome (HHS). 24680727 2014
dbSNP: rs104894342
rs104894342
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia. 15590700 2005
dbSNP: rs104894342
rs104894342
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A novel mutation in fibroblast growth factor 23 gene as a cause of tumoral calcinosis. 16030159 2005
dbSNP: rs104894342
rs104894342
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification. 16151858 2005
dbSNP: rs104894343
rs104894343
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification. 16151858 2005
dbSNP: rs104894343
rs104894343
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia. 15590700 2005
dbSNP: rs104894343
rs104894343
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A novel mutation in fibroblast growth factor 23 gene as a cause of tumoral calcinosis. 16030159 2005
dbSNP: rs104894344
rs104894344
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification. 16151858 2005
dbSNP: rs104894344
rs104894344
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT A novel mutation in fibroblast growth factor 23 gene as a cause of tumoral calcinosis. 16030159 2005
dbSNP: rs104894344
rs104894344
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.800 GeneticVariation UNIPROT An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia. 15590700 2005
dbSNP: rs104894342
rs104894342
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		C 0.800 CausalMutation CLINVAR
dbSNP: rs104894343
rs104894343
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		G 0.800 CausalMutation CLINVAR
dbSNP: rs104894344
rs104894344
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		A 0.800 CausalMutation CLINVAR
dbSNP: rs772964687
rs772964687
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.700 GeneticVariation UNIPROT A new missense mutation in FGF23 gene in a male with hyperostosis-hyperphosphatemia syndrome (HHS). 24680727 2014
dbSNP: rs772964687
rs772964687
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.700 GeneticVariation UNIPROT A novel mutation in fibroblast growth factor 23 gene as a cause of tumoral calcinosis. 16030159 2005
dbSNP: rs772964687
rs772964687
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.700 GeneticVariation UNIPROT A novel homozygous missense mutation in FGF23 causes Familial Tumoral Calcinosis associated with disseminated visceral calcification. 16151858 2005
dbSNP: rs772964687
rs772964687
Entrez Id: 8074
Gene Symbol: FGF23
FGF23
CUI: C4693863
Disease:
TUMORAL CALCINOSIS, HYPERPHOSPHATEMIC, FAMILIAL, 2 		0.700 GeneticVariation UNIPROT An FGF23 missense mutation causes familial tumoral calcinosis with hyperphosphatemia. 15590700 2005