Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
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
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs4845625
IL6R
0.851 0.080 1 154449591 intron variant T/C snv 0.60 9
rs1168013
DOCK7
1.000 0.120 1 62531167 intron variant C/G;T snv 6
rs10889332
DOCK7
1.000 0.120 1 62485187 3 prime UTR variant C/T snv 0.39 4
rs11206517
PCSK9
1.000 0.120 1 55060755 intron variant T/C;G snv 4
rs4846913
GALNT2
1.000 0.120 1 230158968 intron variant C/A;T snv 4
rs1057156731
LMNA
0.925 0.120 1 156137730 missense variant T/A snv 3
rs59914820
LMNA
0.925 0.160 1 156115000 missense variant C/G;T snv 3
rs7552841
PCSK9
0.925 0.160 1 55053079 intron variant C/T snv 0.32 3
rs11122316
GALNT2
1.000 0.120 1 230101356 intron variant A/G snv 0.42 2
rs11576175
CTSS
1.000 1 150754918 intron variant G/A snv 7.2E-02 2
rs1997947
GALNT2
1.000 0.120 1 230148017 intron variant G/A snv 0.78 2
rs2760537
GALNT2
1.000 0.120 1 230190666 intron variant G/A snv 0.23 2
rs2808607
EGLN1
1.000 0.080 1 231405228 intron variant G/A snv 0.56 2
rs41284589
SPATA1 ; GNG5
1.000 0.040 1 84506243 5 prime UTR variant G/A snv 5.4E-02 2
rs615563
PCSK9
1.000 0.120 1 55060623 intron variant A/C;G snv 2
rs10911205
LAMC1
1 183040142 intron variant C/A snv 0.33 1
rs10911232
LAMC1
1 183083398 intron variant C/T snv 0.33 1
rs672059
LAMC2
1 183193404 intron variant G/A snv 0.57 1
rs1260326
GCKR
0.645 0.600 2 27508073 missense variant T/C;G snv 0.63; 4.0E-06 0.68 81