Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1344039930
rs1344039930
MYOC ; MYOCOS
1 1.000 0.040 1 171636359 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs1351328951
rs1351328951
MYOC ; MYOCOS
1 1.000 0.040 1 171636584 missense variant A/G snv 8.0E-06 0.700 0
dbSNP: rs199746824
rs199746824
MYOC
6 0.807 0.040 1 171652139 missense variant C/G;T snv 4.0E-06; 1.6E-05 0.700 0
dbSNP: rs200120115
rs200120115
MYOC
1 1.000 0.040 1 171652236 missense variant G/A snv 1.5E-04 1.3E-04 0.700 0
dbSNP: rs200208925
rs200208925
MYOC
2 0.925 0.040 1 171652454 missense variant A/G snv 6.4E-05 2.1E-05 0.700 0
dbSNP: rs2234927
rs2234927
MYOC ; MYOCOS
4 0.851 0.040 1 171638703 missense variant G/A;C snv 4.0E-06; 7.6E-04 0.700 0
dbSNP: rs566289099
rs566289099
MYOC ; MYOCOS
6 0.807 0.080 1 171636310 missense variant G/A snv 2.0E-05 3.5E-05 0.700 0
dbSNP: rs74315329
rs74315329
MYOC ; MYOCOS
15 0.732 0.240 1 171636338 stop gained G/A snv 1.1E-03 8.7E-04 0.700 0
dbSNP: rs748621461
rs748621461
MYOC ; MYOCOS
2 0.925 0.040 1 171636542 missense variant C/T snv 3.2E-05 2.1E-05 0.700 0
dbSNP: rs757769997
rs757769997
MYOC ; MYOCOS
1 1.000 0.040 1 171636709 missense variant C/A snv 2.5E-05 7.0E-06 0.700 0
dbSNP: rs771122834
rs771122834
MYOC ; MYOCOS
1 1.000 0.040 1 171636032 missense variant G/A snv 2.0E-05 1.4E-05 0.700 0
dbSNP: rs79204362
rs79204362
CYP1B1
10 0.763 0.120 2 38071251 missense variant C/T snv 5.8E-03 1.7E-03 0.700 0
dbSNP: rs982896610
rs982896610
MYOC ; MYOCOS
1 1.000 0.040 1 171636659 missense variant C/T snv 0.700 0
dbSNP: rs1200513428
rs1200513428
MYOC ; MYOCOS
1 1.000 0.040 1 171636140 missense variant C/T snv 4.0E-06 0.700 1.000 20 1997 2007
dbSNP: rs121909193
rs121909193
MYOC ; MYOCOS
2 0.925 0.040 1 171636349 missense variant C/A snv 0.800 1.000 20 1997 2007
dbSNP: rs121909194
rs121909194
MYOC ; MYOCOS
3 0.882 0.040 1 171636302 missense variant C/G snv 0.800 1.000 20 1997 2007
dbSNP: rs137853277
rs137853277
MYOC ; MYOCOS
3 0.925 0.040 1 171636382 missense variant G/A snv 7.0E-04 3.1E-04 0.700 1.000 20 1997 2007
dbSNP: rs139122673
rs139122673
MYOC ; MYOCOS
1 1.000 0.040 1 171636562 missense variant G/A;T snv 1.2E-05; 5.9E-04 0.700 1.000 20 1997 2007
dbSNP: rs140967767
rs140967767
MYOC ; MYOCOS
2 0.925 0.040 1 171636106 missense variant G/A snv 1.9E-04 3.4E-04 0.700 1.000 20 1997 2007
dbSNP: rs201573718
rs201573718
MYOC ; MYOCOS
1 1.000 0.040 1 171636175 missense variant C/T snv 2.4E-05 5.6E-05 0.700 1.000 20 1997 2007
dbSNP: rs28936694
rs28936694
MYOC ; MYOCOS
2 0.925 0.040 1 171636244 missense variant C/A snv 1.6E-05 0.700 1.000 20 1997 2007
dbSNP: rs554235897
rs554235897
MYOC ; MYOCOS
2 0.925 0.040 1 171636028 missense variant T/C snv 2.8E-05 0.700 1.000 20 1997 2007
dbSNP: rs61745146
rs61745146
MYOC ; MYOCOS
1 1.000 0.040 1 171636386 missense variant C/G;T snv 9.3E-04 0.700 1.000 20 1997 2007
dbSNP: rs74315328
rs74315328
MYOC ; MYOCOS
6 0.807 0.120 1 171636131 missense variant A/G snv 0.800 1.000 20 1997 2007
dbSNP: rs74315330
rs74315330
MYOC ; MYOCOS
9 0.776 0.080 1 171636331 missense variant G/A snv 0.800 1.000 20 1997 2007