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: rs281865228
rs281865228
BEST1 ; LOC107984334
1 1.000 0.080 11 61955769 missense variant T/C;G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865229
rs281865229
BEST1 ; LOC107984334
1 1.000 0.080 11 61955771 missense variant C/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865230
rs281865230
BEST1 ; LOC107984334
1 1.000 0.080 11 61955774 missense variant T/C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865231
rs281865231
BEST1 ; LOC107984334
1 1.000 0.080 11 61955780 missense variant G/C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865232
rs281865232
BEST1 ; LOC107984334
1 1.000 0.080 11 61955782 missense variant C/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865233
rs281865233
BEST1 ; LOC107984334
1 1.000 0.080 11 61955869 missense variant C/G snv 7.0E-06 0.700 1.000 18 1998 2011
dbSNP: rs281865234
rs281865234
BEST1 ; LOC107984334
1 1.000 0.080 11 61955873 missense variant G/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865235
rs281865235
BEST1 ; LOC107984334
1 1.000 0.080 11 61955889 missense variant T/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865237
rs281865237
BEST1 ; LOC107984334
1 1.000 0.080 11 61956988 missense variant G/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865240
rs281865240
BEST1 ; LOC107984334
1 1.000 0.080 11 61957413 missense variant T/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865242
rs281865242
BEST1 ; LOC107984334
1 1.000 0.080 11 61957420 missense variant C/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865243
rs281865243
BEST1 ; LOC107984334
1 1.000 0.080 11 61957421 missense variant T/A;C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865244
rs281865244
BEST1 ; LOC107984334
1 1.000 0.080 11 61957443 missense variant T/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865245
rs281865245
BEST1 ; LOC107984334
1 1.000 0.080 11 61957453 missense variant G/A;C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865246
rs281865246
BEST1 ; LOC107984334
1 1.000 0.080 11 61957460 missense variant C/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865247
rs281865247
BEST1 ; LOC107984334
1 1.000 0.080 11 61958153 missense variant C/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865248
rs281865248
BEST1 ; LOC107984334
1 1.000 0.080 11 61958259 missense variant C/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865250
rs281865250
BEST1 ; LOC107984334
2 0.925 0.080 11 61959507 missense variant C/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865251
rs281865251
BEST1 ; LOC107984334
1 1.000 0.080 11 61959510 missense variant C/G snv 0.700 1.000 18 1998 2011
dbSNP: rs281865253
rs281865253
BEST1 ; LOC107984334
1 1.000 0.080 11 61959514 missense variant T/C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865254
rs281865254
BEST1 ; LOC107984334
1 1.000 0.080 11 61959516 missense variant A/C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865255
rs281865255
BEST1 ; LOC107984334
2 0.925 0.080 11 61959517 missense variant A/G snv 0.800 1.000 18 1998 2011
dbSNP: rs281865257
rs281865257
BEST1 ; LOC107984334
1 1.000 0.080 11 61959523 missense variant T/C snv 0.700 1.000 18 1998 2011
dbSNP: rs281865259
rs281865259
BEST1 ; LOC107984334
1 1.000 0.080 11 61959531 missense variant G/A snv 0.700 1.000 18 1998 2011
dbSNP: rs281865261
rs281865261
BEST1 ; LOC107984334
1 1.000 0.080 11 61959533 missense variant T/C;G snv 0.700 1.000 18 1998 2011