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: rs1676486
rs1676486
7 0.851 0.120 1 102888582 missense variant A/G;T snv 0.80; 4.0E-06 0.020 1.000 2 2007 2013
dbSNP: rs2615977
rs2615977
3 0.925 0.080 1 102986836 intron variant A/C snv 0.27 0.010 < 0.001 1 2013 2013
dbSNP: rs10490571
rs10490571
5 0.827 0.320 2 102100877 intron variant C/T snv 0.29 0.010 1.000 1 2019 2019
dbSNP: rs762704392
rs762704392
1 1.000 0.080 2 112836208 missense variant C/T snv 2.4E-05 2.1E-05 0.010 1.000 1 2011 2011
dbSNP: rs956730
rs956730
2 0.925 0.120 2 102141656 intron variant G/A snv 0.42 0.010 1.000 1 2019 2019
dbSNP: rs1400328611
rs1400328611
TNF
1 1.000 0.080 6 31575804 frameshift variant AG/- del 0.010 1.000 1 2011 2011
dbSNP: rs1799971
rs1799971
95 0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 0.010 1.000 1 2012 2012
dbSNP: rs62413038
rs62413038
1 1.000 0.080 6 63952008 intron variant T/A;G snv 0.49 0.010 1.000 1 2019 2019
dbSNP: rs9406328
rs9406328
2 1.000 0.080 6 169234915 splice region variant G/A snv 0.37 0.31 0.010 1.000 1 2008 2008
dbSNP: rs9450607
rs9450607
1 1.000 0.080 6 64025138 intron variant A/G snv 0.32 0.010 1.000 1 2019 2019
dbSNP: rs6651255
rs6651255
1 1.000 0.080 8 129711546 intron variant T/A;C snv 0.710 1.000 1 2017 2017
dbSNP: rs10998461
rs10998461
1 1.000 0.080 10 68856761 intron variant G/T snv 0.44 0.010 1.000 1 2020 2020
dbSNP: rs10998468
rs10998468
1 1.000 0.080 10 68867495 intron variant T/C snv 0.22 0.010 1.000 1 2020 2020
dbSNP: rs4472827
rs4472827
1 1.000 0.080 10 68892516 intron variant G/A snv 0.33 0.010 1.000 1 2020 2020
dbSNP: rs7903209
rs7903209
1 1.000 0.080 10 68868826 intron variant C/T snv 0.28 0.010 1.000 1 2020 2020
dbSNP: rs10767664
rs10767664
16 0.752 0.400 11 27704439 intron variant T/A snv 0.83 0.010 1.000 1 2018 2018
dbSNP: rs11030064
rs11030064
1 1.000 0.080 11 27596469 intron variant C/T snv 0.41 0.010 1.000 1 2018 2018
dbSNP: rs11030096
rs11030096
3 0.925 0.160 11 27643996 intron variant T/A;C snv 0.010 1.000 1 2018 2018
dbSNP: rs11030104
rs11030104
12 0.790 0.240 11 27662970 intron variant A/G snv 0.16 0.010 1.000 1 2018 2018
dbSNP: rs6265
rs6265
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.010 1.000 1 2018 2018
dbSNP: rs7481311
rs7481311
2 0.925 0.160 11 27561582 intron variant T/C snv 0.75 0.010 1.000 1 2018 2018
dbSNP: rs11066028
rs11066028
2 1.000 0.080 12 111807366 intron variant A/C snv 0.45 0.010 1.000 1 2018 2018
dbSNP: rs375081888
rs375081888
2 0.925 0.120 12 117331048 missense variant C/T snv 2.4E-05 7.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs671
rs671
116 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 0.010 1.000 1 2018 2018
dbSNP: rs7296651
rs7296651
2 0.925 0.160 12 111809150 intron variant C/A;G snv 0.010 1.000 1 2018 2018