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: rs10905284
rs10905284
4 0.882 0.200 10 8073399 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1129844
rs1129844
13 0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 0.010 < 0.001 1 2011 2011
dbSNP: rs13181
rs13181
134 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 0.010 1.000 1 2017 2017
dbSNP: rs1391371
rs1391371
2 0.925 0.160 6 32636021 intron variant A/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1888909
rs1888909
4 0.882 0.200 9 6197392 downstream gene variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs2280540
rs2280540
1 1.000 0.120 11 192997 intron variant G/A;C;T snv 0.010 1.000 1 2018 2018
dbSNP: rs2428494
rs2428494
5 0.827 0.160 6 31354420 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs338598
rs338598
1 1.000 0.120 19 41195623 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs3939286
rs3939286
12 0.776 0.360 9 6210099 regulatory region variant T/A;C snv 0.010 1.000 1 2010 2010
dbSNP: rs4807542
rs4807542
3 1.000 0.120 19 1104079 synonymous variant G/A;C snv 0.22; 1.8E-05 0.700 1.000 1 2019 2019
dbSNP: rs759412116
rs759412116
55 0.581 0.640 19 45352210 missense variant C/G;T snv 4.0E-06; 6.0E-05 0.010 1.000 1 2017 2017
dbSNP: rs7817
rs7817
2 0.925 0.200 7 112475603 3 prime UTR variant C/G;T snv 0.010 1.000 1 2015 2015
dbSNP: rs8046011
rs8046011
3 1.000 0.120 16 11226805 downstream gene variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs74767530
rs74767530
5 0.851 0.320 7 117627537 stop gained C/T snv 5.6E-05 4.9E-05 0.010 1.000 1 1993 1993
dbSNP: rs34210653
rs34210653
8 0.807 0.280 17 4632019 missense variant G/A snv 2.7E-02 1.7E-02 0.710 1.000 1 2019 2019
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.020 1.000 2 2009 2018
dbSNP: rs113795008
rs113795008
1 1.000 0.120 11 192836 intron variant A/G snv 0.17 0.010 1.000 1 2018 2018
dbSNP: rs828618
rs828618
2 0.925 0.160 3 98822789 intron variant G/A snv 0.28 0.22 0.010 1.000 1 2012 2012
dbSNP: rs7302200
rs7302200
6 0.851 0.200 12 56055651 regulatory region variant G/A snv 0.23 0.700 1.000 1 2019 2019
dbSNP: rs62408225
rs62408225
2 1.000 0.120 6 90246690 intron variant A/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs17718444
rs17718444
1 1.000 0.120 3 71450250 intron variant C/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs1050152
rs1050152
10 0.776 0.480 5 132340627 missense variant C/T snv 0.29 0.28 0.700 1.000 1 2019 2019
dbSNP: rs3129878
rs3129878
6 0.807 0.360 6 32440958 intron variant A/C snv 0.30 0.010 1.000 1 2012 2012
dbSNP: rs174535
rs174535
19 0.776 0.280 11 61783884 missense variant T/A;C;G snv 0.38 0.32 0.700 1.000 1 2019 2019
dbSNP: rs1444782
rs1444782
5 0.851 0.240 10 9016708 intergenic variant G/A snv 0.35 0.700 1.000 1 2019 2019