Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs118203990
rs118203990
1.000 22 46337925 missense variant T/C snv 4.0E-06
CUI: C3278664
Disease: LIVER FAILURE, INFANTILE, TRANSIENT
LIVER FAILURE, INFANTILE, TRANSIENT
0.800 1.000 1 2009 2009
dbSNP: rs118203991
rs118203991
1.000 22 46353809 missense variant G/A snv
CUI: C3278664
Disease: LIVER FAILURE, INFANTILE, TRANSIENT
LIVER FAILURE, INFANTILE, TRANSIENT
0.800 1.000 1 2009 2009
dbSNP: rs387907022
rs387907022
0.925 22 46353829 missense variant G/A snv 1.7E-04 1.1E-04
CUI: C3278664
Disease: LIVER FAILURE, INFANTILE, TRANSIENT
LIVER FAILURE, INFANTILE, TRANSIENT
0.700 1.000 4 2009 2015
dbSNP: rs118203992
rs118203992
1.000 22 46335766 start lost T/A;C;G snv 6.9E-06
CUI: C3278664
Disease: LIVER FAILURE, INFANTILE, TRANSIENT
LIVER FAILURE, INFANTILE, TRANSIENT
0.700 0
dbSNP: rs1490906786
rs1490906786
1.000 22 46355445 frameshift variant C/-;CC delins
CUI: C3278664
Disease: LIVER FAILURE, INFANTILE, TRANSIENT
LIVER FAILURE, INFANTILE, TRANSIENT
0.700 0
dbSNP: rs766314948
rs766314948
1.000 22 46352316 missense variant T/C snv 4.0E-06
CUI: C3278664
Disease: LIVER FAILURE, INFANTILE, TRANSIENT
LIVER FAILURE, INFANTILE, TRANSIENT
0.700 0
dbSNP: rs863224242
rs863224242
1.000 22 46355521 frameshift variant -/C delins
CUI: C3278664
Disease: LIVER FAILURE, INFANTILE, TRANSIENT
LIVER FAILURE, INFANTILE, TRANSIENT
0.700 0