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: rs9277412
rs9277412
1 1.000 0.120 6 33083912 non coding transcript exon variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277421
rs9277421
1 1.000 0.120 6 33084043 intron variant G/A snv 0.37 0.700 1.000 1 2011 2011
dbSNP: rs9277424
rs9277424
1 1.000 0.120 6 33084088 intron variant A/C snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277426
rs9277426
2 0.925 0.200 6 33084133 intron variant C/A;G snv 0.700 1.000 1 2011 2011
dbSNP: rs9277431
rs9277431
1 1.000 0.120 6 33084251 intron variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277432
rs9277432
2 0.925 0.200 6 33084295 intron variant A/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277434
rs9277434
1 1.000 0.120 6 33084409 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9277437
rs9277437
2 0.925 0.200 6 33084473 intron variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277450
rs9277450
1 1.000 0.120 6 33084918 intron variant T/G snv 4.3E-02 0.700 1.000 1 2011 2011
dbSNP: rs9277458
rs9277458
2 0.925 0.200 6 33085390 intron variant A/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9277460
rs9277460
1 1.000 0.120 6 33085475 intron variant G/A snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277463
rs9277463
2 0.925 0.200 6 33085530 intron variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277468
rs9277468
2 0.925 0.200 6 33085678 intron variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277469
rs9277469
2 0.925 0.200 6 33085691 intron variant G/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277470
rs9277470
1 1.000 0.120 6 33085700 intron variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9277477
rs9277477
2 0.925 0.200 6 33085995 intron variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs9277479
rs9277479
2 0.925 0.200 6 33086012 intron variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277492
rs9277492
2 0.925 0.200 6 33086205 intron variant G/A;C snv 4.4E-06; 0.28 0.700 1.000 1 2011 2011
dbSNP: rs9277497
rs9277497
1 1.000 0.120 6 33086314 intron variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277515
rs9277515
2 0.925 0.200 6 33086491 intron variant C/A;T snv 8.3E-03; 7.4E-06 0.700 1.000 1 2011 2011
dbSNP: rs9277518
rs9277518
1 1.000 0.120 6 33086525 intron variant T/C snv 1.0E-02 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277533
rs9277533
2 0.925 0.200 6 33086944 3 prime UTR variant C/T snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277534
rs9277534
7 0.790 0.280 6 33087030 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277538
rs9277538
2 0.925 0.200 6 33087270 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2011 2011
dbSNP: rs9277540
rs9277540
2 0.925 0.200 6 33087346 3 prime UTR variant A/G snv 0.38 0.700 1.000 1 2011 2011