Source: ALL

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: rs5030860
rs5030860
PAH
0.925 0.120 12 102840474 missense variant T/C snv 3.7E-04 2.4E-04
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1995 1995
dbSNP: rs62507283
rs62507283
PAH
12 102852941 missense variant C/A;G;T snv
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2018 2018
dbSNP: rs62507329
rs62507329
PAH
1.000 0.120 12 102843761 missense variant G/A;T snv 4.0E-06
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1998 1998
dbSNP: rs62508577
rs62508577
PAH
1.000 0.120 12 102855150 missense variant G/A snv
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2009 2009
dbSNP: rs62508721
rs62508721
PAH
1.000 0.120 12 102855222 missense variant T/C snv
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1997 1997
dbSNP: rs62514903
rs62514903
PAH
0.925 0.120 12 102894812 missense variant G/A snv 4.0E-06 1.4E-05
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1998 1998
dbSNP: rs62514927
rs62514927
PAH
1.000 0.120 12 102855231 missense variant T/C snv 1.2E-05 7.0E-06
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1991 1991
dbSNP: rs62516092
rs62516092
PAH
1.000 0.120 12 102844359 missense variant G/C snv 1.0E-04 1.3E-04
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2000 2000
dbSNP: rs62516103
rs62516103
PAH
1.000 0.120 12 102843662 missense variant C/G snv 2.0E-05 7.0E-06
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2002 2002
dbSNP: rs62642926
rs62642926
PAH
1.000 0.120 12 102912842 missense variant G/C snv 9.5E-05 9.1E-05
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2000 2000
dbSNP: rs62642932
rs62642932
PAH
1.000 0.120 12 102852882 missense variant C/T snv 4.0E-06
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2000 2000
dbSNP: rs62642937
rs62642937
PAH
0.925 0.120 12 102843706 missense variant G/A snv 4.4E-04 3.6E-04
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1994 1994
dbSNP: rs62644499
rs62644499
PAH
0.925 0.120 12 102840472 missense variant C/T snv 1.1E-04 1.1E-04
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1998 1998
dbSNP: rs76151636
rs76151636
0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2019 2019
dbSNP: rs76212747
rs76212747
PAH
0.925 0.120 12 102852923 missense variant A/G;T snv 4.8E-04; 2.4E-05
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1994 1994
dbSNP: rs76542238
rs76542238
PAH
1.000 0.120 12 102839194 missense variant G/T snv 8.0E-06 1.4E-05
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1998 1998
dbSNP: rs76687508
rs76687508
PAH
0.925 0.120 12 102852936 missense variant G/A snv 1.4E-04 8.4E-05
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2004 2004
dbSNP: rs773526027
rs773526027
PAH
1.000 0.120 12 102840497 missense variant T/C snv 1.2E-05 2.1E-05
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2019 2019
dbSNP: rs796052017
rs796052017
PAH
0.925 0.120 12 102852922 missense variant CA/TG mnv
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 1994 1994
dbSNP: rs79635844
rs79635844
PAH
1.000 0.120 12 102866623 missense variant A/G snv
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2018 2018
dbSNP: rs79931499
rs79931499
PAH
1.000 0.120 12 102840477 missense variant C/G;T snv 4.0E-06; 5.6E-05
CUI: C0031485
Disease: Phenylketonurias
Phenylketonurias
0.010 1.000 1 2018 2018