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: rs74315331
rs74315331
MYOC ; MYOCOS
3 0.882 0.040 1 171636010 missense variant A/C;T snv 0.800 1.000 20 1997 2007
dbSNP: rs74315332
rs74315332
MYOC ; MYOCOS
3 0.882 0.040 1 171636000 missense variant G/T snv 0.800 1.000 20 1997 2007
dbSNP: rs74315334
rs74315334
MYOC ; MYOCOS
4 0.851 0.040 1 171636341 missense variant C/T snv 0.800 1.000 20 1997 2007
dbSNP: rs74315335
rs74315335
MYOC ; MYOCOS
1 1.000 0.040 1 171636430 missense variant T/C snv 0.800 1.000 20 1997 2007
dbSNP: rs74315336
rs74315336
MYOC ; MYOCOS
4 0.851 0.040 1 171636173 missense variant T/C snv 0.800 1.000 20 1997 2007
dbSNP: rs74315338
rs74315338
MYOC ; MYOCOS
3 0.882 0.040 1 171636143 missense variant A/G snv 0.800 1.000 20 1997 2007
dbSNP: rs74315339
rs74315339
MYOC
6 0.807 0.120 1 171652468 missense variant C/A snv 9.8E-04 1.3E-04 0.800 1.000 20 1997 2007
dbSNP: rs74315340
rs74315340
MYOC ; MYOCOS
1 1.000 0.040 1 171636706 missense variant C/T snv 0.800 1.000 20 1997 2007
dbSNP: rs74315341
rs74315341
MYOC ; MYOCOS
4 0.851 0.040 1 171636686 missense variant C/T snv 0.800 1.000 20 1997 2007
dbSNP: rs754237376
rs754237376
MYOC ; MYOCOS
3 0.882 0.080 1 171636161 missense variant C/T snv 4.8E-05 2.1E-05 0.700 1.000 20 1997 2007
dbSNP: rs755246983
rs755246983
MYOC
2 0.925 0.040 1 171652539 missense variant A/G snv 8.0E-06; 4.0E-06 0.700 1.000 20 1997 2007
dbSNP: rs764005392
rs764005392
MYOC
1 1.000 0.040 1 171652368 missense variant G/A snv 7.6E-05 7.7E-05 0.700 1.000 20 1997 2007
dbSNP: rs998968146
rs998968146
MYOC ; MYOCOS
1 1.000 0.040 1 171636261 missense variant G/C snv 0.700 1.000 20 1997 2007