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: rs199476339
rs199476339
1 1.000 0.120 22 50627721 missense variant G/A;T snv 0.700 0
dbSNP: rs199476340
rs199476340
1 1.000 0.120 22 50627686 missense variant C/G snv 0.700 0
dbSNP: rs199476341
rs199476341
1 1.000 0.120 22 50626878 missense variant C/G;T snv 8.0E-06 0.700 0
dbSNP: rs199476342
rs199476342
1 1.000 0.120 22 50626594 missense variant T/C snv 0.700 0
dbSNP: rs199476343
rs199476343
1 1.000 0.120 22 50626221 missense variant C/G snv 7.0E-06 0.700 0
dbSNP: rs199476344
rs199476344
1 1.000 0.120 22 50625657 missense variant A/T snv 0.700 0
dbSNP: rs199476346
rs199476346
1 1.000 0.120 22 50627689 missense variant C/A;T snv 0.700 0
dbSNP: rs199476347
rs199476347
1 1.000 0.120 22 50626246 missense variant C/T snv 1.4E-05 0.700 0
dbSNP: rs199476348
rs199476348
1 1.000 0.120 22 50627046 missense variant A/G snv 0.700 0
dbSNP: rs199476350
rs199476350
1 1.000 0.120 22 50627680 missense variant C/T snv 0.700 0
dbSNP: rs199476351
rs199476351
1 1.000 0.120 22 50627571 missense variant A/G snv 0.700 0
dbSNP: rs199476353
rs199476353
1 1.000 0.120 22 50627345 missense variant G/C snv 0.700 0
dbSNP: rs199476354
rs199476354
1 1.000 0.120 22 50626760 missense variant G/A snv 7.0E-06 0.700 0
dbSNP: rs199476360
rs199476360
1 1.000 0.120 22 50626208 stop gained C/A;G;T snv 4.1E-06; 4.1E-06; 4.1E-06 0.700 0
dbSNP: rs199476363
rs199476363
1 1.000 0.120 22 50627341 missense variant C/T snv 0.700 0
dbSNP: rs199476364
rs199476364
1 1.000 0.120 22 50627270 missense variant C/T snv 0.700 0
dbSNP: rs199476365
rs199476365
1 1.000 0.120 22 50627171 missense variant C/A;G;T snv 8.3E-06 0.700 0
dbSNP: rs199476367
rs199476367
1 1.000 0.120 22 50626690 missense variant G/A;T snv 0.700 0
dbSNP: rs199476369
rs199476369
1 1.000 0.120 22 50625936 missense variant C/G snv 0.700 0
dbSNP: rs199476370
rs199476370
1 1.000 0.120 22 50625633 missense variant G/A;C snv 1.2E-05; 4.0E-06 0.700 0
dbSNP: rs199476371
rs199476371
2 0.925 0.120 22 50627338 missense variant GA/AG mnv 0.700 0
dbSNP: rs199476372
rs199476372
1 1.000 0.120 22 50626942 missense variant C/G snv 0.700 0
dbSNP: rs199476373
rs199476373
1 1.000 0.120 22 50627198 missense variant G/C snv 0.700 0
dbSNP: rs199476376
rs199476376
1 1.000 0.120 22 50625594 missense variant G/A snv 8.0E-06 0.700 0
dbSNP: rs199476377
rs199476377
1 1.000 0.120 22 50627166 missense variant C/G;T snv 4.2E-06 0.700 0