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: rs1020608562
rs1020608562
9 0.807 0.160 3 46373738 missense variant T/C snv 4.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs1369619997
rs1369619997
1 2 8731746 missense variant G/C snv 4.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs14158
rs14158
5 0.851 0.160 19 11131368 synonymous variant G/A snv 0.24 0.22 0.010 1.000 1 2013 2013
dbSNP: rs1799864
rs1799864
68 0.572 0.680 3 46357717 missense variant G/A snv 0.13 0.12 0.010 1.000 1 2002 2002
dbSNP: rs1800629
rs1800629
TNF
169 0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 0.010 1.000 1 2019 2019
dbSNP: rs1800871
rs1800871
108 0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 0.010 1.000 1 2010 2010
dbSNP: rs241447
rs241447
11 0.827 0.280 6 32828974 missense variant T/C snv 0.31 0.26 0.010 1.000 1 2020 2020
dbSNP: rs3732378
rs3732378
48 0.620 0.720 3 39265671 missense variant G/A snv 0.14 0.12 0.010 1.000 1 2005 2005
dbSNP: rs3732379
rs3732379
38 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 0.010 1.000 1 2005 2005
dbSNP: rs374596032
rs374596032
1 2 8813255 missense variant A/C;G snv 4.0E-06; 8.0E-06 0.010 1.000 1 2009 2009
dbSNP: rs763059810
rs763059810
41 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 0.010 1.000 1 2002 2002
dbSNP: rs767830104
rs767830104
13 0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2005 2005
dbSNP: rs909253
rs909253
34 0.641 0.600 6 31572536 intron variant A/G;T snv 0.010 1.000 1 2019 2019
dbSNP: rs919266
rs919266
1 19 17403506 intron variant T/C;G snv 0.010 1.000 1 2016 2016
dbSNP: rs12198173
rs12198173
9 0.827 0.240 6 32059031 intron variant G/A snv 0.10 0.700 1.000 1 2009 2009
dbSNP: rs1233579
rs1233579
3 0.925 0.160 6 28744886 intergenic variant A/G snv 7.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs1235162
rs1235162
6 0.827 0.280 6 29569447 intron variant A/G snv 6.0E-02 0.700 1.000 1 2009 2009
dbSNP: rs13194504
rs13194504
3 0.925 0.120 6 28662914 intergenic variant G/A snv 5.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs2248462
rs2248462
10 0.807 0.240 6 31479019 downstream gene variant G/A snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs2284178
rs2284178
6 0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 0.700 1.000 1 2009 2009
dbSNP: rs2516509
rs2516509
7 0.882 0.160 6 31482217 intron variant T/C snv 0.19 0.700 1.000 1 2009 2009
dbSNP: rs2844511
rs2844511
10 0.807 0.200 6 31422007 intron variant A/G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2844513
rs2844513
6 0.925 0.120 6 31420437 intron variant G/A snv 0.53 0.700 1.000 1 2009 2009
dbSNP: rs2894207
rs2894207
8 0.882 0.160 6 31295974 intron variant T/C snv 0.20 0.700 1.000 1 2009 2009
dbSNP: rs3093662
rs3093662
TNF
9 0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 0.700 1.000 1 2009 2009