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: 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
dbSNP: rs3117143
rs3117143
4 0.882 0.160 6 29063365 intron variant C/A snv 5.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs3130380
rs3130380
10 0.807 0.280 6 30311353 intron variant G/A snv 6.6E-02 0.700 1.000 1 2009 2009
dbSNP: rs3131093
rs3131093
3 0.925 0.160 6 28869660 intergenic variant C/T snv 7.1E-02 0.700 1.000 1 2009 2009
dbSNP: rs3815087
rs3815087
8 0.851 0.200 6 31125810 5 prime UTR variant G/A snv 0.25 0.700 1.000 1 2009 2009
dbSNP: rs3823418
rs3823418
8 0.925 0.120 6 31133165 intron variant G/A snv 0.23 0.700 1.000 1 2009 2009
dbSNP: rs4118325
rs4118325
1 1 107035210 intergenic variant G/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs4324798
rs4324798
8 0.790 0.240 6 28808340 intergenic variant G/A snv 7.2E-02 0.700 1.000 1 2009 2009
dbSNP: rs527476195
rs527476195
6 0.925 0.120 6 31133165 intron variant G/A snv 0.700 1.000 1 2009 2009
dbSNP: rs6467710
rs6467710
1 7 137519073 intron variant G/A;C snv 0.800 1.000 1 2011 2011
dbSNP: rs7756521
rs7756521
5 1.000 6 30880476 intron variant T/C snv 0.25 0.700 1.000 1 2009 2009
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: rs9368699
rs9368699
8 0.851 0.200 6 31834764 non coding transcript exon variant T/C snv 3.2E-02 0.700 1.000 1 2009 2009