Source: CURATED

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1057517201
rs1057517201
FAH
1.000 0.120 15 80177584 splice donor variant G/A snv
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1057517341
rs1057517341
FAH
1.000 0.120 15 80153066 frameshift variant C/- delins
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1057517436
rs1057517436
FAH
1.000 0.120 15 80173083 frameshift variant TC/- delins 7.0E-06
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs121965076
rs121965076
FAH
1.000 0.120 15 80181069 stop gained G/T snv 2.4E-05 2.1E-05
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555440522
rs1555440522
FAH
1.000 0.120 15 80159754 splice acceptor variant A/G snv
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555440603
rs1555440603
FAH
1.000 0.120 15 80160408 splice acceptor variant A/G snv
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555441251
rs1555441251
FAH
1.000 0.120 15 80168050 splice acceptor variant A/G snv
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555441272
rs1555441272
FAH
1.000 0.120 15 80168149 splice donor variant TG/- delins
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555441597
rs1555441597
FAH
1.000 0.120 15 80172250 splice donor variant T/G snv
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555441852
rs1555441852
FAH
1.000 0.120 15 80175022 frameshift variant -/TGGCCCCTGCC delins
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555441861
rs1555441861
FAH
1.000 0.120 15 80175060 frameshift variant -/T delins
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555442289
rs1555442289
FAH
1.000 0.120 15 80180122 splice acceptor variant A/C snv
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555442385
rs1555442385
FAH
1.000 0.120 15 80181040 splice acceptor variant A/G snv
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs370686447
rs370686447
FAH
1.000 0.120 15 80168052 stop gained G/A;T snv 1.2E-05; 4.0E-06
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs533540262
rs533540262
FAH
1.000 0.120 15 80172238 missense variant C/A;T snv 4.0E-06; 1.6E-05
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs772895065
rs772895065
FAH
1.000 0.120 15 80153137 splice donor variant T/A;C snv 1.2E-05
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs779642226
rs779642226
FAH
1.000 0.120 15 80162319 frameshift variant T/- del 1.4E-05
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs886044640
rs886044640
FAH
1.000 0.120 15 80180126 stop gained C/A snv 7.0E-06
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.700 0
dbSNP: rs1555441595
rs1555441595
FAH
1.000 0.120 15 80172242 missense variant T/G snv
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.710 1.000 14 1992 2009
dbSNP: rs769550316
rs769550316
FAH
1.000 0.120 15 80173016 stop gained C/T snv 1.2E-05 2.1E-05
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.710 1.000 1 1996 2012
dbSNP: rs80338894
rs80338894
FAH
1.000 0.120 15 80158170 missense variant G/A;T snv 4.0E-06; 6.4E-05
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.800 1.000 22 1992 2016
dbSNP: rs80338898
rs80338898
FAH
1.000 0.120 15 80173089 missense variant C/T snv 1.7E-04 5.6E-05
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.800 1.000 18 1992 2013
dbSNP: rs80338900
rs80338900
FAH
1.000 0.120 15 80180172 missense variant G/A snv 7.2E-05 6.3E-05
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.800 1.000 18 1992 2014
dbSNP: rs778387055
rs778387055
FAH
1.000 0.120 15 80168093 missense variant T/G snv 4.0E-06
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.800 1.000 17 1992 2011
dbSNP: rs121965074
rs121965074
FAH
0.882 0.120 15 80162282 missense variant C/A snv 4.0E-06
CUI: C0268490
Disease: Tyrosinemia, Type I
Tyrosinemia, Type I
0.800 1.000 16 1992 2009