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
rs1131691014
TP53
0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs878854066
TP53
0.439 0.800 17 7676153 missense variant GG/AC mnv 213
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs3212227
IL12B
0.566 0.840 5 159315942 3 prime UTR variant T/G snv 0.26 65
rs1024611 0.568 0.800 17 34252769 upstream gene variant A/G snv 0.28 63
rs8099917 0.581 0.600 19 39252525 upstream gene variant T/G snv 0.16 60
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs568408
IL12A ; IL12A-AS1
0.649 0.600 3 159995680 3 prime UTR variant G/A snv 0.16 29
rs3742330
DICER1
0.662 0.640 14 95087025 3 prime UTR variant A/G snv 8.7E-02 24
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs7120118
NR1H3
0.716 0.360 11 47264739 intron variant T/C snv 0.38 18
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs1057035
DICER1
0.763 0.440 14 95087805 3 prime UTR variant T/C snv 0.26 12
rs7895833 0.742 0.440 10 67863299 upstream gene variant G/A;C snv 12
rs2297235
GSTO2
0.752 0.320 10 104274733 5 prime UTR variant A/G snv 0.22 11
rs7069102
SIRT1
0.790 0.440 10 67903362 intron variant C/G snv 0.64 10
rs360719
IL18 ; LOC107987164 ; TEX12
0.790 0.480 11 112165426 non coding transcript exon variant A/G snv 0.25 7
rs9657182
IDO1
0.851 0.280 8 39908329 intron variant C/G;T snv 6
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs3512
FAN1 ; MTMR10
0.925 0.160 15 30942802 3 prime UTR variant G/C snv 0.27 4
rs1272951905
MTHFSD
0.925 0.160 16 86532210 missense variant C/T snv 2.1E-05 3
rs1382597320
ATN1
0.882 0.160 12 6934305 missense variant A/G snv 7.0E-06 3
rs2742976
E2F2
0.882 0.240 1 23531510 upstream gene variant T/A;G snv 3
rs10881578
RXRA
0.925 0.240 9 134340689 intron variant A/G snv 0.32 2