Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1396171148
rs1396171148
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0023890
Disease:
Liver Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs1396171148
rs1396171148
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0270685
Disease:
Cerebral calcification
G 0.700 CausalMutation CLINVAR
dbSNP: rs1396171148
rs1396171148
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0206061
Disease:
Pneumonia, Interstitial
G 0.700 CausalMutation CLINVAR
dbSNP: rs1419129874
rs1419129874
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0002940
Disease:
Aneurysm
G 0.700 CausalMutation CLINVAR
dbSNP: rs1419129874
rs1419129874
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0206061
Disease:
Pneumonia, Interstitial
G 0.700 CausalMutation CLINVAR
dbSNP: rs1419129874
rs1419129874
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0270685
Disease:
Cerebral calcification
G 0.700 CausalMutation CLINVAR
dbSNP: rs1419129874
rs1419129874
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C3150910
Disease:
Brain calcification Rajab type
0.700 GeneticVariation UNIPROT
dbSNP: rs1419129874
rs1419129874
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0023890
Disease:
Liver Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs1466642025
rs1466642025
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0023890
Disease:
Liver Cirrhosis
G 0.700 CausalMutation CLINVAR
dbSNP: rs1466642025
rs1466642025
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0270685
Disease:
Cerebral calcification
G 0.700 CausalMutation CLINVAR
dbSNP: rs1466642025
rs1466642025
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0002940
Disease:
Aneurysm
G 0.700 CausalMutation CLINVAR
dbSNP: rs1466642025
rs1466642025
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0206061
Disease:
Pneumonia, Interstitial
G 0.700 CausalMutation CLINVAR
dbSNP: rs1553549333
rs1553549333
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C4225400
Disease:
INTERSTITIAL LUNG AND LIVER DISEASE
TT 0.700 GeneticVariation CLINVAR
dbSNP: rs1553549333
rs1553549333
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C3150910
Disease:
Brain calcification Rajab type
TT 0.700 CausalMutation CLINVAR
dbSNP: rs1553553086
rs1553553086
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0042580
Disease:
Vesico-Ureteral Reflux
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553553086
rs1553553086
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0206061
Disease:
Pneumonia, Interstitial
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553553086
rs1553553086
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0023890
Disease:
Liver Cirrhosis
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553553086
rs1553553086
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0002940
Disease:
Aneurysm
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553553086
rs1553553086
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0270685
Disease:
Cerebral calcification
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553553086
rs1553553086
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0026827
Disease:
Muscle hypotonia
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553553086
rs1553553086
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C1837260
Disease:
Prominent forehead
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553553086
rs1553553086
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C4021780
Disease:
Abnormality of the liver
T 0.700 CausalMutation CLINVAR
dbSNP: rs1553554543
rs1553554543
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0270685
Disease:
Cerebral calcification
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553554543
rs1553554543
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0002940
Disease:
Aneurysm
C 0.700 CausalMutation CLINVAR
dbSNP: rs1553554543
rs1553554543
Entrez Id: 10056
Gene Symbol: FARSB
FARSB
CUI: C0023890
Disease:
Liver Cirrhosis
C 0.700 CausalMutation CLINVAR