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
rs2910164
MIR3142HG ; MIR146A
0.447 0.880 5 160485411 mature miRNA variant C/G snv 0.71; 4.1E-06 0.70 193
rs1048943
CYP1A1
0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs2274223
PLCE1
0.620 0.400 10 94306584 missense variant A/G snv 0.28 0.31 40
rs2241880
SCARNA5 ; ATG16L1
0.627 0.600 2 233274722 missense variant A/G snv 0.45 0.44 37
rs1864183
ATG10
0.742 0.240 5 82253397 missense variant C/T snv 0.52 0.40 12
rs3759601
ATG2B
0.790 0.240 14 96311131 missense variant G/C snv 0.36 0.32 7
rs2238135
VDR
0.882 0.160 12 47884407 intron variant C/G snv 0.26 4
rs7834169 0.925 0.120 8 27052774 upstream gene variant C/G snv 0.16 3
rs1816158
MIR100HG
0.925 0.200 11 122155752 intron variant C/A;T snv 3
rs1373756 1.000 0.120 18 52259936 intergenic variant C/T snv 0.24 2
rs221236 1.000 0.120 7 157529938 downstream gene variant G/A snv 0.96 2
rs16914640
CLEC2D
1.000 0.120 12 9669791 missense variant C/G;T snv 0.14; 4.0E-06 2
rs221636
LIN28B
1.000 0.120 6 105082089 3 prime UTR variant T/A snv 0.82 2
rs1271546630
MPO
1.000 0.120 17 58277848 missense variant G/A;C snv 2