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: rs16835979
rs16835979
6 0.851 0.120 4 4633549 intron variant C/A snv 0.20 0.030 1.000 3 2014 2016
dbSNP: rs6824295
rs6824295
6 0.851 0.120 4 4612553 intron variant C/T snv 0.20 0.030 1.000 3 2014 2016
dbSNP: rs870142
rs870142
7 0.851 0.120 4 4646320 intron variant C/G;T snv 0.020 1.000 2 2015 2016
dbSNP: rs1340513
rs1340513
4 0.882 0.120 9 6977633 intron variant G/A snv 0.75 0.010 1.000 1 2010 2010
dbSNP: rs2298444
rs2298444
3 0.925 0.120 11 72221370 intron variant T/C snv 0.27 0.010 1.000 1 2019 2019
dbSNP: rs804280
rs804280
6 0.882 0.120 8 11755189 intron variant C/A;G snv 0.010 1.000 1 2015 2015
dbSNP: rs104893907
rs104893907
3 1.000 5 173232776 stop gained A/C;T snv 0.010 1.000 1 2006 2006
dbSNP: rs1345146178
rs1345146178
1 5 173233003 stop gained G/A snv 0.010 1.000 1 2017 2017
dbSNP: rs1213930919
rs1213930919
9 0.882 0.120 2 178577785 stop gained G/A snv 0.700 0
dbSNP: rs132630297
rs132630297
6 0.925 0.280 X 134425256 stop gained C/A;T snv 0.700 0
dbSNP: rs149830411
rs149830411
15 0.827 0.360 17 46171276 stop gained G/A snv 5.2E-05 5.6E-05 0.700 0
dbSNP: rs1554093433
rs1554093433
4 0.925 0.080 5 173232833 stop gained G/T snv 0.700 0
dbSNP: rs1555226315
rs1555226315
4 0.925 0.120 12 114398639 stop gained C/T snv 0.700 0
dbSNP: rs1555932766
rs1555932766
9 0.882 0.080 X 41210540 stop gained C/T snv 0.700 0
dbSNP: rs367557471
rs367557471
4 1.000 0.120 8 60822055 stop gained C/A;T snv 5.2E-05 7.0E-05 0.700 0
dbSNP: rs387906846
rs387906846
19 0.807 0.280 1 26773716 stop gained C/G;T snv 0.700 0
dbSNP: rs398123278
rs398123278
4 0.925 0.120 6 49459376 stop gained G/A snv 1.6E-05 2.8E-05 0.700 0
dbSNP: rs730881014
rs730881014
15 0.776 0.360 1 155904494 stop gained A/C;G;T snv 0.700 0
dbSNP: rs759125480
rs759125480
16 0.827 0.160 5 123377409 stop gained G/A snv 1.6E-05 0.700 0
dbSNP: rs912001256
rs912001256
17 0.851 0.240 17 63947062 stop gained G/A snv 0.700 0
dbSNP: rs121908557
rs121908557
23 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 0.700 1.000 2 2004 2008
dbSNP: rs104893900
rs104893900
2 1.000 5 173233011 missense variant G/A snv 0.010 1.000 1 2003 2003
dbSNP: rs104894073
rs104894073
8 0.827 0.080 8 11750213 missense variant G/A;C;T snv 0.010 1.000 1 2019 2019
dbSNP: rs1060499548
rs1060499548
27 0.724 0.440 9 130872961 missense variant G/A snv 0.700 1.000 1 2017 2017
dbSNP: rs111862418
rs111862418
1 7 35204548 missense variant A/C;T snv 0.010 1.000 1 2015 2015