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
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
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs20417
PACERR ; PTGS2
0.576 0.600 1 186681189 non coding transcript exon variant C/G;T snv 57
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs2234922
EPHX1
0.630 0.440 1 225838705 missense variant A/G;T snv 0.19; 2.8E-05 42
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs2295080
MTOR
0.695 0.320 1 11262571 upstream gene variant G/C;T snv 20
rs1476413
MTHFR
0.790 0.360 1 11792243 intron variant C/G;T snv 4.0E-06; 0.26 0.23 10
rs1194611372
S100A11
0.763 0.320 1 152032679 missense variant A/C snv 9
rs760805
RUNX3 ; LOC107984932
0.776 0.240 1 24925432 intron variant A/T snv 0.42 9
rs1883965
MTOR
0.807 0.160 1 11262099 intron variant A/G snv 0.63 8
rs2067079
GAS5 ; SNORA103 ; SNORD80 ; SNORD77 ; SNORD81 ; SNORD44 ; SNORD78 ; SNORD47 ; SNORD79
0.807 0.240 1 173866073 non coding transcript exon variant C/T snv 0.22 0.18 7
rs6790
GAS5 ; SNORD47 ; SNORD78 ; SNORD79 ; SNORD81 ; SNORD80 ; SNORD44
0.790 0.320 1 173865494 non coding transcript exon variant G/A snv 8.9E-02 7
rs8679
PARP1
0.790 0.200 1 226360853 3 prime UTR variant A/G snv 0.16 7
rs10759
RGS4
0.851 0.160 1 163076561 3 prime UTR variant G/A;T snv 4
rs11249206
RUNX3 ; LOC105376878
0.851 0.160 1 24951491 intron variant C/T snv 0.48 4
rs140241283
MTHFR
0.882 0.120 1 11796249 start lost A/G;T snv 4.0E-06; 4.0E-06 3
rs1484761909
GSTM1 ; GSTM2
0.882 0.120 1 109688224 missense variant A/G snv 3.0E-05 3.8E-05 3
rs197414
DDX20
0.882 0.120 1 111766501 missense variant C/A;T snv 0.12; 4.0E-06 3
rs3219493
MUTYH
0.882 0.120 1 45330597 intron variant G/C snv 0.92 0.93 3
rs8444
CERS2
0.882 0.120 1 150966095 3 prime UTR variant G/A snv 0.35 3
rs1056836
CYP1B1
0.581 0.680 2 38071060 missense variant G/C snv 0.51 58