Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2424913
DNMT3B
0.708 0.440 20 32786453 intron variant C/T snv 0.56 0.53 18
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs28936670
NKX2-5
0.708 0.280 5 173235011 missense variant G/A snv 3.4E-03 1.1E-02 17
rs3733890
BHMT ; DMGDH
0.708 0.480 5 79126136 missense variant G/A snv 0.30 0.28 16
rs1569686
DNMT3B
0.752 0.400 20 32779273 intron variant G/A;C;T snv 15
rs1237063529
CBS
0.752 0.360 21 43058894 missense variant T/G snv 5.6E-06 13
rs1532268
MTRR
0.776 0.280 5 7878066 missense variant C/T snv 0.31 0.32 12
rs1359880314
SLC19A1
0.763 0.320 21 45534541 synonymous variant C/T snv 1.6E-05 2.8E-05 12
rs587781858
TP53
0.742 0.360 17 7669671 missense variant C/A;G;T snv 4.0E-06; 4.0E-06 12
rs2305764
MYO9B
0.776 0.360 19 17203024 non coding transcript exon variant G/A snv 0.52 0.50 10
rs1457092
MYO9B
0.790 0.320 19 17193427 intron variant C/A snv 0.44 8
rs2435357
RET
0.790 0.240 10 43086608 intron variant T/C snv 0.79 8
rs2071421
ARSA
0.790 0.200 22 50625988 missense variant T/C snv 0.17 0.19 7
rs121912594
CPS1
0.882 0.160 2 210675762 missense variant A/C snv 7
rs12325817
PEMT
0.807 0.320 17 17583205 intron variant C/A;G;T snv 7
rs104893904
NKX2-5
0.807 0.160 5 173235023 missense variant C/G snv 1.1E-03 7.1E-04 6
rs562625029
CBS
0.827 0.280 21 43058192 stop gained G/A snv 5
rs12676
CHDH
0.827 0.240 3 53823776 missense variant A/C;T snv 0.77 5
rs1465444723
TCN2
0.827 0.240 22 30610886 missense variant A/G snv 4.0E-06 5
rs373667881
TRIB1
0.827 0.160 8 125431222 missense variant G/A;T snv 1.1E-03 5
rs3774207
CRELD1
0.851 0.160 3 9943972 synonymous variant C/T snv 0.27 0.38 4
rs73118372
CRELD1
0.851 0.160 3 9943989 missense variant T/C;G snv 2.6E-02; 6.8E-05 4
rs755981922
CRELD1
0.851 0.160 3 9943440 missense variant G/A snv 8.0E-06 2.1E-05 4
rs9878047
CRELD1
0.851 0.160 3 9943773 intron variant T/C snv 0.38 4
rs1323833193
EGF
0.851 0.160 4 109994859 missense variant C/G snv 4.0E-06 4