Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs759317757
OTUD6B
0.807 0.280 8 91078416 frameshift variant TTAAC/- delins 12
rs148173957
LOC105378976
1.000 0.040 5 56078195 intron variant TT/- del 8.2E-02 2
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs2282679
GC
0.645 0.480 4 71742666 intron variant T/G snv 0.21 38
rs730882223
TSEN15
0.851 0.120 1 184054736 missense variant T/G snv 4
rs386833981
FBXL3 ; CLN5
0.925 0.120 13 77000517 missense variant T/G snv 3
rs765078446
CILK1
0.925 0.040 6 53013900 missense variant T/G snv 2.0E-05 2.1E-05 3
rs9596863
LINC00558
1.000 0.040 13 53860512 intron variant T/G snv 0.11 2
rs193929353
KCNJ11
0.882 0.120 11 17387206 missense variant T/C;G snv 4
rs12483428
MIR155HG
1.000 0.040 21 25561470 upstream gene variant T/C;G snv 1
rs1051740
EPHX1
0.592 0.760 1 225831932 missense variant T/C snv 0.32 0.27 56
rs886039469
KCNMA1-AS1 ; KCNMA1
0.701 0.560 10 76891709 missense variant T/C snv 35
rs776746
CYP3A5 ; ZSCAN25
0.724 0.400 7 99672916 splice acceptor variant T/C snv 0.72 21
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs7439366
UGT2B7
0.752 0.320 4 69098620 missense variant T/C snv 0.56 0.57 16
rs193929337
KCNJ11
0.827 0.160 11 17387937 missense variant T/C snv 6
rs2274924
TRPM6
0.851 0.160 9 74761731 missense variant T/C snv 0.20 0.23 6
rs2307441
POLG
0.882 0.080 15 89318595 missense variant T/C snv 2.9E-02 2.7E-02 6
rs7127507
BDNF-AS ; BDNF
0.827 0.080 11 27693337 intron variant T/C snv 0.34 6
rs137852776
EFHC1
0.827 0.080 6 52452799 missense variant T/C snv 3.5E-03 2.4E-03 5
rs796053134
SCN2A
0.827 0.080 2 165374737 missense variant T/C snv 5
rs1057518988
GRIN2B
0.925 0.040 12 13571859 missense variant T/C snv 3
rs200533370
SYN1
0.882 0.160 X 47574285 missense variant T/C snv 1.1E-03 1.4E-02 3
rs1178326
HDAC9
1.000 0.040 7 18195234 intron variant T/C snv 3.9E-02 2
rs137853333
KCNMA1
0.925 0.080 10 77090433 missense variant T/C snv 7.0E-06 2