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: rs142572218
rs142572218
ADAMTS13
2 0.925 0.080 9 133454548 missense variant C/A;T snv 8.3E-04 0.810 1.000 23 2001 2018
dbSNP: rs281875299
rs281875299
ADAMTS13
2 0.925 0.080 9 133440344 missense variant C/T snv 1.2E-05 0.810 1.000 22 2001 2019
dbSNP: rs121908475
rs121908475
ADAMTS13
1 1.000 0.080 9 133442504 missense variant C/T snv 4.0E-06 2.1E-05 0.810 1.000 21 2001 2011
dbSNP: rs121908470
rs121908470
ADAMTS13
1 1.000 0.080 9 133426246 missense variant C/T snv 8.0E-06 2.8E-05 0.810 1.000 20 2001 2011
dbSNP: rs281875302
rs281875302
ADAMTS13
1 1.000 0.080 9 133424410 missense variant G/A snv 4.0E-06 1.4E-05 0.800 1.000 22 2001 2011
dbSNP: rs281875307
rs281875307
ADAMTS13
1 1.000 0.080 9 133442447 missense variant A/G;T snv 8.0E-06; 4.0E-06 0.800 1.000 21 2001 2011
dbSNP: rs121908467
rs121908467
ADAMTS13
1 1.000 0.080 9 133424434 missense variant C/G snv 0.800 1.000 20 2001 2011
dbSNP: rs121908468
rs121908468
ADAMTS13
1 1.000 0.080 9 133448718 missense variant T/G snv 7.0E-06 0.800 1.000 20 2001 2011
dbSNP: rs121908469
rs121908469
ADAMTS13
1 1.000 0.080 9 133424452 missense variant C/A;T snv 4.0E-06; 8.0E-06 2.1E-05 0.800 1.000 20 2001 2011
dbSNP: rs121908471
rs121908471
ADAMTS13
1 1.000 0.080 9 133433478 missense variant G/A snv 0.800 1.000 20 2001 2011
dbSNP: rs121908472
rs121908472
ADAMTS13
1 1.000 0.080 9 133454440 missense variant T/G snv 3.2E-05 1.2E-04 0.800 1.000 20 2001 2011
dbSNP: rs121908473
rs121908473
ADAMTS13
1 1.000 0.080 9 133437895 missense variant A/G snv 4.0E-06 0.800 1.000 20 2001 2011
dbSNP: rs121908474
rs121908474
ADAMTS13
1 1.000 0.080 9 133456138 missense variant G/A snv 7.0E-06 0.800 1.000 20 2001 2011
dbSNP: rs121908477
rs121908477
ADAMTS13
1 1.000 0.080 9 133428750 missense variant G/C;T snv 0.800 1.000 20 2001 2011
dbSNP: rs121908478
rs121908478
ADAMTS13
1 1.000 0.080 9 133428696 missense variant C/T snv 0.800 1.000 20 2001 2011
dbSNP: rs281875287
rs281875287
ADAMTS13
1 1.000 0.080 9 133426236 missense variant C/T snv 8.0E-06 7.0E-06 0.800 1.000 20 2001 2011
dbSNP: rs281875288
rs281875288
ADAMTS13
1 1.000 0.080 9 133432645 missense variant C/A;T snv 1.2E-05; 5.9E-06 0.710 1.000 21 2001 2011
dbSNP: rs148312697
rs148312697
ADAMTS13
2 0.925 0.080 9 133426218 missense variant G/C snv 4.7E-04 4.3E-04 0.710 1.000 7 2009 2016
dbSNP: rs281875285
rs281875285
ADAMTS13
1 1.000 0.080 9 133430025 missense variant A/G;T snv 4.6E-06 0.700 1.000 20 2001 2011
dbSNP: rs281875286
rs281875286
ADAMTS13
1 1.000 0.080 9 133437887 missense variant G/A snv 0.700 1.000 20 2001 2011
dbSNP: rs281875289
rs281875289
ADAMTS13
1 1.000 0.080 9 133426056 missense variant T/C snv 0.700 1.000 20 2001 2011
dbSNP: rs281875290
rs281875290
ADAMTS13
1 1.000 0.080 9 133440373 missense variant G/C snv 4.0E-06 6.3E-05 0.700 1.000 20 2001 2011
dbSNP: rs281875291
rs281875291
ADAMTS13
1 1.000 0.080 9 133425554 missense variant C/T snv 0.700 1.000 20 2001 2011
dbSNP: rs281875292
rs281875292
ADAMTS13
1 1.000 0.080 9 133428642 missense variant T/A snv 0.700 1.000 20 2001 2011
dbSNP: rs281875293
rs281875293
ADAMTS13
1 1.000 0.080 9 133428735 missense variant C/A;G snv 0.700 1.000 20 2001 2011