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
rs3219472
TOE1 ; MUTYH
0.882 0.160 1 45338378 5 prime UTR variant C/T snv 0.26 3
rs4661636
CASP9
0.925 0.160 1 15496566 intron variant C/T snv 0.24 2
rs1035142
FLACC1
0.807 0.200 2 201288355 3 prime UTR variant T/C;G snv 0.54 7
rs11901649
APOB
0.882 0.080 2 21027351 intron variant G/A;C;T snv 3
rs7255
GDF7
0.925 0.080 2 20679060 3 prime UTR variant T/A;C snv 3
rs12465911 0.925 0.080 2 150929228 intergenic variant C/T snv 0.21 2
rs13396805 0.925 0.080 2 150964998 intergenic variant C/T snv 0.20 2
rs2341926 0.925 0.080 2 150927414 intergenic variant A/G snv 0.20 2
rs13429103
LOC107985847
1.000 0.080 2 7377100 intergenic variant G/A snv 0.16 1
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs2687201 0.925 0.080 3 70879779 intergenic variant A/C;G snv 6
rs7632500
LOC107986152
0.925 0.080 3 168007561 downstream gene variant A/G snv 0.17 5
rs4676893 0.882 0.080 3 70868488 intergenic variant A/T snv 0.61 3
rs2687202 0.925 0.080 3 70880832 regulatory region variant T/C snv 0.64 2
rs9823696 0.925 0.080 3 184065565 downstream gene variant A/G;T snv 2
rs11941492
KDR
1.000 0.080 4 55112043 intron variant C/T snv 0.24 2
rs2114039 1.000 0.080 4 54226459 intron variant T/C snv 0.40 2
rs9918259
CEP72 ; TPPP
0.925 0.080 5 662977 3 prime UTR variant C/T snv 2.1E-03 2
rs17708574
PDGFRB
1.000 0.080 5 150141675 intron variant G/A snv 8.2E-02 1
rs2434584 1.000 0.080 5 58270246 intergenic variant G/A snv 0.94 1
rs75783973
TPPP
1.000 0.080 5 668194 intron variant G/A snv 2.9E-04 1
rs1800629
TNF
0.472 0.920 6 31575254 upstream gene variant G/A snv 0.12 0.14 169