Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs35829419
NLRP3
0.689 0.560 1 247425556 missense variant C/A snv 3.9E-02 3.3E-02 23
rs8192284
IL6R
0.724 0.720 1 154454494 missense variant A/C;T snv 19
rs80356814
LMNA
0.732 0.320 1 156138697 synonymous variant C/T snv 8.0E-06 15
rs17465637
MIA3
0.790 0.200 1 222650187 intron variant A/C;G;T snv 0.64; 6.4E-06 11
rs3737787
TSTD1 ; USF1
0.763 0.280 1 161039733 3 prime UTR variant G/A snv 0.21 11
rs3811381
CR1
0.763 0.240 1 207616743 missense variant C/A;G snv 8.0E-06; 0.24 11
rs137852912
PCSK9
0.776 0.120 1 55057454 missense variant G/A;C;T snv 7.2E-05 10
rs374603772
PCSK9
0.776 0.160 1 55058630 missense variant C/T snv 4.4E-05 2.8E-05 9
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs3480
FNDC5
0.807 0.160 1 32862564 3 prime UTR variant G/A snv 0.56 8
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs28942111
PCSK9
0.807 0.120 1 55044016 missense variant T/A snv 7
rs2229238
IL6R
0.851 0.080 1 154465420 3 prime UTR variant T/A;C snv 0.80 5
rs4845617
IL6R-AS1 ; IL6R
0.882 0.080 1 154405422 5 prime UTR variant G/A;C snv 4
rs4845623
IL6R
0.925 0.040 1 154443301 intron variant A/G snv 0.47 4
rs1746661
FNDC5
0.925 0.080 1 32869438 intron variant G/A;T snv 3
rs28942112
PCSK9
0.925 0.040 1 55052400 missense variant T/C snv 3
rs3767140
HSPG2
1.000 0.080 1 21888152 intron variant C/A snv 0.25 3
rs8179183
LEPR
1.000 0.080 1 65610269 missense variant G/C;T snv 3