Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs895819 0.623 0.560 19 13836478 non coding transcript exon variant T/A;C;G snv 0.34 0.38 46
rs6318 0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs763059810 0.623 0.600 2 136115750 missense variant T/C snv 4.0E-06 41
rs777919630
CBS
0.623 0.680 21 43062358 missense variant G/A;T snv 8.0E-06; 4.0E-06 40
rs10889677 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 40
rs58542926 0.630 0.440 19 19268740 missense variant C/T snv 6.5E-02 5.8E-02 42
rs1801725 0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs763351020 0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs1458766475 0.637 0.680 1 169732649 missense variant C/G;T snv 4.0E-06; 4.0E-06 41
rs268
LPL
0.637 0.480 8 19956018 missense variant A/G snv 1.3E-02 1.3E-02 41
rs3732379 0.637 0.680 3 39265765 missense variant C/T snv 0.22 0.22 38
rs4762
AGT
0.637 0.440 1 230710231 missense variant G/A snv 0.12 0.11 35
rs10741657 0.637 0.520 11 14893332 upstream gene variant A/G snv 0.65 34
rs7412 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 47
rs909253 0.641 0.600 6 31572536 intron variant A/G;T snv 34
rs1260326 0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81
rs1256049 0.645 0.560 14 64257333 synonymous variant C/T snv 6.7E-02 6.3E-02 32
rs121917864 0.645 0.520 4 153704936 missense variant C/T snv 8.8E-05 9.8E-05 31
rs5882 0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 35
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs1799889 0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs4673 0.653 0.600 16 88646828 missense variant A/G;T snv 0.70 32
rs11575937 0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs745738344
TNF
0.653 0.600 6 31576786 synonymous variant G/A snv 1.6E-05 1.4E-05 28
rs1799883 0.658 0.440 4 119320747 missense variant T/A;C;G snv 0.73 36