FAS, Fas cell surface death receptor, 355

N. diseases: 754; N. variants: 47
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs267607122
rs267607122
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA 		C 0.700 CausalMutation CLINVAR
dbSNP: rs28929498
rs28929498
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA 		T 0.700 CausalMutation CLINVAR
dbSNP: rs28929498
rs28929498
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT
dbSNP: rs606231361
rs606231361
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA 		T 0.700 CausalMutation CLINVAR
dbSNP: rs606231362
rs606231362
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA 		GT 0.700 CausalMutation CLINVAR
dbSNP: rs606231363
rs606231363
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA 		C 0.700 CausalMutation CLINVAR
dbSNP: rs606231364
rs606231364
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA 		A 0.700 CausalMutation CLINVAR
dbSNP: rs606231364
rs606231364
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin 		0.700 GeneticVariation UNIPROT
dbSNP: rs606231365
rs606231365
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA 		GAAAATTCAAACTTCAGAAAT 0.700 CausalMutation CLINVAR
dbSNP: rs606231366
rs606231366
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA 		AT 0.700 CausalMutation CLINVAR
dbSNP: rs758835365
rs758835365
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0024305
Disease:
Lymphoma, Non-Hodgkin 		0.700 GeneticVariation UNIPROT
dbSNP: rs1554852244
rs1554852244
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0026827
Disease:
Muscle hypotonia 		TCATG 0.700 CausalMutation CLINVAR Mutations in Fas associated with human lymphoproliferative syndrome and autoimmunity. 7539157 1995
dbSNP: rs121913076
rs121913076
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. 7540117 1995
dbSNP: rs121913078
rs121913078
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. 7540117 1995
dbSNP: rs121913079
rs121913079
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. 7540117 1995
dbSNP: rs121913080
rs121913080
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. 7540117 1995
dbSNP: rs121913081
rs121913081
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. 7540117 1995
dbSNP: rs121913086
rs121913086
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. 7540117 1995
dbSNP: rs201072885
rs201072885
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Dominant interfering Fas gene mutations impair apoptosis in a human autoimmune lymphoproliferative syndrome. 7540117 1995
dbSNP: rs121913076
rs121913076
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity. 8929361 1996
dbSNP: rs121913078
rs121913078
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity. 8929361 1996
dbSNP: rs121913079
rs121913079
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity. 8929361 1996
dbSNP: rs121913080
rs121913080
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity. 8929361 1996
dbSNP: rs121913081
rs121913081
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity. 8929361 1996
dbSNP: rs121913086
rs121913086
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome 		0.700 GeneticVariation UNIPROT Fas gene mutations in the Canale-Smith syndrome, an inherited lymphoproliferative disorder associated with autoimmunity. 8929361 1996