Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs80338897
rs80338897
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
T 0.800 CausalMutation CLINVAR

dbSNP: rs121965078
rs121965078
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
G 0.800 CausalMutation CLINVAR

dbSNP: rs121965077
rs121965077
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
G 0.800 CausalMutation CLINVAR

dbSNP: rs121965074
rs121965074
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
A 0.800 CausalMutation CLINVAR

dbSNP: rs121965073
rs121965073
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
T 0.800 CausalMutation CLINVAR

dbSNP: rs970505762
rs970505762
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
T 0.700 CausalMutation CLINVAR

dbSNP: rs886044640
rs886044640
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
A 0.700 GeneticVariation CLINVAR

dbSNP: rs786204683
rs786204683
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
T 0.700 CausalMutation CLINVAR

dbSNP: rs779642226
rs779642226
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
A 0.700 GeneticVariation CLINVAR

dbSNP: rs772895065
rs772895065
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
A 0.700 GeneticVariation CLINVAR

dbSNP: rs772895065
rs772895065
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
A 0.700 CausalMutation CLINVAR

dbSNP: rs772895065
rs772895065
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
C 0.700 GeneticVariation CLINVAR

dbSNP: rs533540262
rs533540262
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
T 0.700 GeneticVariation CLINVAR

dbSNP: rs370686447
rs370686447
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
A 0.700 CausalMutation CLINVAR

dbSNP: rs370686447
rs370686447
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
A 0.700 GeneticVariation CLINVAR

dbSNP: rs1555442385
rs1555442385
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555442289
rs1555442289
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555441861
rs1555441861
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
AT 0.700 GeneticVariation CLINVAR

dbSNP: rs1555441852
rs1555441852
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
AGGCCCCTGCCT 0.700 GeneticVariation CLINVAR

dbSNP: rs1555441597
rs1555441597
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555441597
rs1555441597
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
G 0.700 CausalMutation CLINVAR

dbSNP: rs1555441272
rs1555441272
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
C 0.700 GeneticVariation CLINVAR

dbSNP: rs1555441272
rs1555441272
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
C 0.700 CausalMutation CLINVAR

dbSNP: rs1555441251
rs1555441251
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
G 0.700 GeneticVariation CLINVAR

dbSNP: rs1555440603
rs1555440603
FAH
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
G 0.700 GeneticVariation CLINVAR