Source: CLINVAR

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: rs727503963
rs727503963
1.000 0.080 1 23808187 missense variant T/C snv 4.0E-06 4.2E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.800 1.000 9 1996 2009
dbSNP: rs121964997
rs121964997
1.000 0.080 1 23820532 missense variant C/T snv 2.4E-05 4.2E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.800 1.000 2 1996 2009
dbSNP: rs121964998
rs121964998
1.000 0.080 1 23804441 missense variant C/T snv
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.800 1.000 0 1996 2009
dbSNP: rs763494292
rs763494292
0.925 0.080 1 23820545 stop gained C/A snv 4.8E-05 6.3E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 1.000 7 1997 2017
dbSNP: rs786205431
rs786205431
1.000 0.080 1 23802526 frameshift variant AA/- delins 4.0E-06
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 1.000 4 1998 2009
dbSNP: rs1409716731
rs1409716731
1.000 0.080 1 23825389 frameshift variant C/- del 2.1E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 1.000 2 2003 2017
dbSNP: rs1212444447
rs1212444447
1.000 0.080 1 23825385 stop gained G/A snv 1.2E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 1.000 1 2017 2017
dbSNP: rs752137615
rs752137615
1.000 0.080 1 23817521 frameshift variant AG/- delins 1.4E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 1.000 1 1993 1993
dbSNP: rs764264834
rs764264834
1.000 0.080 1 23810791 frameshift variant GA/- delins 1.2E-05 7.0E-06
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 1.000 1 2013 2013
dbSNP: rs770225915
rs770225915
1.000 0.080 1 23820533 stop gained G/A snv 4.0E-06 1.4E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 1.000 1 1998 1998
dbSNP: rs890995574
rs890995574
1.000 0.080 1 23816737 stop gained G/A snv
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 1.000 1 2001 2001
dbSNP: rs112508527
rs112508527
1.000 0.080 1 23810769 stop gained A/C;G;T snv 7.6E-05; 4.0E-06
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs1184002840
rs1184002840
1.000 0.080 1 23816737 frameshift variant G/- del 4.0E-06
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs1302190999
rs1302190999
1.000 0.080 1 23825413 start lost C/A snv
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs1324641233
rs1324641233
1.000 0.080 1 23825355 splice donor variant C/A;G snv 6.3E-06
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs1425615804
rs1425615804
1.000 0.080 1 23804413 stop gained A/T snv 7.0E-06
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs1553131955
rs1553131955
1.000 0.080 1 23808325 splice acceptor variant T/C snv
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs1553132209
rs1553132209
1.000 0.080 1 23810798 missense variant A/T snv
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs1553132520
rs1553132520
1.000 0.080 1 23814274 frameshift variant T/- delins
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs1553133042
rs1553133042
1.000 0.080 1 23820532 frameshift variant -/G delins
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs200189529
rs200189529
1.000 0.080 1 23810796 stop gained G/A;C snv 1.2E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0
dbSNP: rs765198174
rs765198174
1.000 0.080 1 23804472 stop gained G/A;T snv 1.2E-05 2.1E-05
CUI: C0268601
Disease: HMG CoA lyase deficiency
HMG CoA lyase deficiency
0.700 0