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: rs121912288
rs121912288
1 0.925 0.120 X 154773152 missense variant C/T snv 0.820 1.000 13 1998 2019
dbSNP: rs121912292
rs121912292
1 0.925 0.120 X 154765478 missense variant C/G snv 0.800 1.000 10 1998 2014
dbSNP: rs121912293
rs121912293
1 0.925 0.120 X 154765465 missense variant T/G snv 0.800 1.000 10 1998 2014
dbSNP: rs121912294
rs121912294
1 1.000 0.120 X 154765949 missense variant CT/TA mnv 0.800 1.000 10 1998 2014
dbSNP: rs121912295
rs121912295
1 0.925 0.120 X 154774651 missense variant G/A snv 0.800 1.000 10 1998 2014
dbSNP: rs121912304
rs121912304
1 0.925 0.120 X 154765505 missense variant C/T snv 0.800 1.000 5 1999 2014
dbSNP: rs121912305
rs121912305
1 0.925 0.120 X 154766313 missense variant A/G snv 0.800 1.000 4 1999 2014
dbSNP: rs28936072
rs28936072
1 0.851 0.200 X 154765472 missense variant T/C snv 0.800 1.000 1 2011 2011
dbSNP: rs121912287
rs121912287
1 1.000 0.120 X 154765525 missense variant CT/TC mnv 0.700 1.000 10 1998 2014
dbSNP: rs121912289
rs121912289
1 0.925 0.120 X 154774672 missense variant C/T snv 0.700 1.000 10 1998 2014
dbSNP: rs121912290
rs121912290
1 0.925 0.120 X 154770792 missense variant C/G;T snv 0.700 1.000 10 1998 2014
dbSNP: rs121912291
rs121912291
1 0.925 0.120 X 154770808 missense variant G/A snv 0.700 1.000 10 1998 2014
dbSNP: rs121912296
rs121912296
1 0.925 0.120 X 154765474 missense variant A/G snv 0.700 1.000 10 1998 2014
dbSNP: rs121912297
rs121912297
1 0.925 0.120 X 154765931 missense variant A/G snv 0.700 1.000 10 1998 2014
dbSNP: rs121912298
rs121912298
1 0.925 0.120 X 154773144 missense variant G/A snv 0.700 1.000 10 1998 2014
dbSNP: rs121912299
rs121912299
1 0.925 0.120 X 154774650 missense variant G/A snv 0.700 1.000 10 1998 2014
dbSNP: rs121912300
rs121912300
1 0.925 0.120 X 154773143 missense variant T/C snv 0.700 1.000 10 1998 2014
dbSNP: rs121912301
rs121912301
1 0.925 0.120 X 154765929 missense variant G/C snv 0.700 1.000 10 1998 2014
dbSNP: rs121912302
rs121912302
1 0.925 0.120 X 154765480 missense variant G/A snv 0.700 1.000 10 1998 2014
dbSNP: rs121912303
rs121912303
1 0.925 0.120 X 154762970 missense variant C/T snv 0.700 1.000 10 1998 2014
dbSNP: rs121912306
rs121912306
1 0.925 0.120 X 154765949 missense variant C/T snv 0.700 1.000 10 1998 2014
dbSNP: rs2728726
rs2728726
1 0.925 0.120 X 154770804 missense variant C/A;G snv 0.700 1.000 1 2011 2011