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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs61747728
NPHS2
0.701 0.240 1 179557079 missense variant C/T snv 3.0E-02 2.8E-02 20
rs121913059
CFH
0.716 0.280 1 196747245 missense variant C/T snv 1.4E-04 1.9E-04 16
rs5355
C1orf112 ; SELE
0.742 0.240 1 169726729 missense variant G/A snv 4.5E-02 3.3E-02 14
rs74315342
NPHS2
0.763 0.120 1 179561327 missense variant C/T snv 6.0E-04 5.3E-04 10
rs2229569
SELL ; C1orf112
0.790 0.360 1 169704697 missense variant G/A;T snv 0.21; 3.2E-05 8
rs267734 0.925 0.120 1 150979001 upstream gene variant T/C snv 0.14 7
rs379489
CFH
0.851 0.200 1 196724321 intron variant A/G snv 0.65 4
rs515299
CFH
0.925 0.080 1 196737547 missense variant G/A;C;T snv 4.8E-05; 1.7E-02 4
rs1933182 1.000 0.080 1 109457216 intergenic variant A/C snv 0.63 3
rs12134854
SLC44A5
1.000 0.080 1 75671921 intron variant T/C snv 0.27 2
rs12137135 0.925 0.080 1 22348728 intergenic variant A/C;G snv 2
rs2490391
SDCCAG8
1.000 0.080 1 243306367 3 prime UTR variant A/C snv 0.50 2
rs2802723
SDCCAG8
0.925 0.080 1 243335010 intron variant T/C;G snv 2
rs28415528
THEM4
1.000 0.080 1 151907285 intron variant G/A snv 0.33 2
rs6587640
S100A10
1.000 0.080 1 151982754 downstream gene variant C/T snv 0.37 2
rs6657658 1.000 0.080 1 151967388 regulatory region variant T/C snv 0.33 2
rs76963882
SLC44A5
1.000 0.080 1 75702239 intron variant T/C snv 0.25 2
rs10783124 1.000 0.080 1 99937719 intergenic variant A/G snv 2.9E-02 1
rs12032578
LINC00624
1.000 0.080 1 147339048 intron variant T/C snv 4.9E-02 1
rs6672843
SDCCAG8
1.000 0.080 1 243316789 missense variant G/A snv 8.8E-05 2.8E-04 1