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: rs199422295
rs199422295
3 0.882 0.120 5 1279376 missense variant C/T snv 0.010 1.000 1 2006 2006
dbSNP: rs11209026
rs11209026
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.010 < 0.001 1 2009 2009
dbSNP: rs11465797
rs11465797
2 1.000 0.040 1 67200769 missense variant C/A snv 0.010 1.000 1 2009 2009
dbSNP: rs10818488
rs10818488
8 0.776 0.360 9 120942809 regulatory region variant A/G snv 0.51 0.010 < 0.001 1 2015 2015
dbSNP: rs1051740
rs1051740
56 0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 0.010 1.000 1 2016 2016
dbSNP: rs2234922
rs2234922
42 0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 0.010 1.000 1 2016 2016
dbSNP: rs1800469
rs1800469
78 0.547 0.760 19 41354391 intron variant A/G snv 0.69 0.010 1.000 1 2017 2017
dbSNP: rs2069762
rs2069762
IL2
23 0.672 0.560 4 122456825 upstream gene variant A/C snv 0.24 0.010 < 0.001 1 2017 2017
dbSNP: rs2317130
rs2317130
1 1.000 0.040 19 41355769 intron variant C/G;T snv 0.010 1.000 1 2017 2017
dbSNP: rs510432
rs510432
11 0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 0.010 1.000 1 2019 2019
dbSNP: rs573775
rs573775
4 0.851 0.320 6 106316991 intron variant G/A snv 0.34 0.010 1.000 1 2019 2019
dbSNP: rs803360
rs803360
1 1.000 0.040 6 106318254 intron variant G/A;C snv 0.010 1.000 1 2019 2019