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: rs1057517829
rs1057517829
1 1.000 0.200 2 31531376 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs1060499834
rs1060499834
1 1.000 0.200 2 31580690 stop gained G/A snv 8.6E-06 0.700 0
dbSNP: rs1200261940
rs1200261940
1 1.000 0.200 2 31531384 stop gained G/A;T snv 0.700 0
dbSNP: rs1331249320
rs1331249320
1 1.000 0.200 2 31533681 missense variant C/T snv 0.700 0
dbSNP: rs1340425455
rs1340425455
1 1.000 0.200 2 31533768 splice acceptor variant T/A;C snv 0.700 0
dbSNP: rs1351269392
rs1351269392
1 1.000 0.200 2 31580647 missense variant C/T snv 4.7E-06 7.0E-06 0.700 0
dbSNP: rs1553323033
rs1553323033
1 1.000 0.200 2 31526232 frameshift variant G/- delins 0.700 0
dbSNP: rs1553323036
rs1553323036
1 1.000 0.200 2 31526236 missense variant T/C snv 0.700 0
dbSNP: rs1553323488
rs1553323488
1 1.000 0.200 2 31529322 missense variant G/A snv 0.700 0
dbSNP: rs1553329427
rs1553329427
4 0.851 0.200 2 31580683 frameshift variant A/- del 0.700 0
dbSNP: rs1553329443
rs1553329443
1 1.000 0.200 2 31580696 missense variant C/A snv 0.700 0
dbSNP: rs201175894
rs201175894
1 1.000 0.200 2 31580630 missense variant A/C;G snv 8.1E-05; 1.0E-05 0.700 0
dbSNP: rs587776566
rs587776566
1 1.000 0.200 2 31531448 inframe deletion ATT/- del 0.700 0
dbSNP: rs587776567
rs587776567
1 1.000 0.200 2 31526208 frameshift variant T/- del 0.700 0
dbSNP: rs750444774
rs750444774
1 1.000 0.200 2 31580732 missense variant C/G snv 2.1E-05 1.4E-05 0.700 0
dbSNP: rs759561106
rs759561106
1 1.000 0.200 2 31533615 missense variant G/A snv 6.3E-06 2.1E-05 0.700 0
dbSNP: rs761824859
rs761824859
1 1.000 0.200 2 31580842 missense variant A/G snv 8.3E-06 0.700 0
dbSNP: rs61750397
rs61750397
1 1.000 0.200 2 31529459 splice acceptor variant T/G snv 2.4E-05 2.8E-05 0.700 1.000 2 1991 1992
dbSNP: rs121434245
rs121434245
3 0.882 0.200 2 31580737 missense variant A/T snv 0.800 1.000 16 1992 2005
dbSNP: rs121434246
rs121434246
2 0.925 0.200 2 31533704 missense variant C/T snv 2.3E-05 2.1E-05 0.800 1.000 16 1992 2005
dbSNP: rs121434247
rs121434247
1 1.000 0.200 2 31531371 missense variant C/T snv 3.1E-05 1.5E-04 0.800 1.000 16 1992 2005
dbSNP: rs121434250
rs121434250
7 0.790 0.200 2 31529419 missense variant C/G;T snv 1.4E-04 1.5E-04 0.800 1.000 16 1992 2005
dbSNP: rs121434252
rs121434252
1 1.000 0.200 2 31529370 missense variant G/C snv 5.6E-05 0.800 1.000 16 1992 2005
dbSNP: rs121434253
rs121434253
1 1.000 0.200 2 31529414 missense variant C/A snv 1.2E-05 0.800 1.000 16 1992 2005
dbSNP: rs145712014
rs145712014
1 1.000 0.200 2 31526227 missense variant G/T snv 2.0E-04 6.4E-04 0.700 1.000 16 1992 2005