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: rs121913076
rs121913076
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA
C 0.700 CausalMutation CLINVAR
dbSNP: rs121913077
rs121913077
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA
T 0.700 CausalMutation CLINVAR
dbSNP: rs121913078
rs121913078
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA
T 0.700 CausalMutation CLINVAR
dbSNP: rs121913080
rs121913080
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA
C 0.700 CausalMutation CLINVAR
dbSNP: rs121913081
rs121913081
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA
T 0.700 CausalMutation CLINVAR
dbSNP: rs121913082
rs121913082
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0007137
Disease:
Squamous cell carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs121913082
rs121913082
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C4016044
Disease:
SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC
G 0.700 CausalMutation CLINVAR
dbSNP: rs121913083
rs121913083
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C4016044
Disease:
SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC
G 0.700 CausalMutation CLINVAR
dbSNP: rs121913083
rs121913083
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0007137
Disease:
Squamous cell carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs121913084
rs121913084
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C4016044
Disease:
SQUAMOUS CELL CARCINOMA, BURN SCAR-RELATED, SOMATIC
C 0.700 CausalMutation CLINVAR
dbSNP: rs121913084
rs121913084
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0007137
Disease:
Squamous cell carcinoma
0.700 GeneticVariation UNIPROT
dbSNP: rs121913085
rs121913085
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA
C 0.700 CausalMutation CLINVAR
dbSNP: rs121913086
rs121913086
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA
T 0.700 CausalMutation CLINVAR
dbSNP: rs1554851718
rs1554851718
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0038002
Disease:
Splenomegaly
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1564686301
rs1564686301
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C2674723
Disease:
RAS-ASSOCIATED AUTOIMMUNE LEUKOPROLIFERATIVE DISORDER
A 0.700 CausalMutation CLINVAR
dbSNP: rs1564691414
rs1564691414
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0018681
Disease:
Headache
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1564691414
rs1564691414
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1564691414
rs1564691414
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0024031
Disease:
Low Back Pain
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1564691414
rs1564691414
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C3808022
Disease:
Episodic abdominal pain
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1564691414
rs1564691414
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0497156
Disease:
Lymphadenopathy
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1564691414
rs1564691414
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C0038002
Disease:
Splenomegaly
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1564691414
rs1564691414
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1263846
Disease:
Attention deficit hyperactivity disorder
G 0.700 GeneticVariation CLINVAR
dbSNP: rs1564696849
rs1564696849
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1328840
Disease:
Autoimmune Lymphoproliferative Syndrome
A 0.700 GeneticVariation CLINVAR
dbSNP: rs2234767
rs2234767
Entrez Id: 59;355
Gene Symbol: ACTA2;FAS
ACTA2;FAS
CUI: C2674950
Disease:
LUNG CANCER, SUSCEPTIBILITY TO
A 0.700 SusceptibilityMutation CLINVAR
dbSNP: rs267607122
rs267607122
Entrez Id: 355
Gene Symbol: FAS
FAS
CUI: C1866119
Disease:
Autoimmune Lymphoproliferative Syndrome, Type IA
A 0.700 CausalMutation CLINVAR