Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6191
NR3C1
0.925 0.040 5 143278591 3 prime UTR variant C/A snv 0.48 4
rs1541665
KCNIP1
1.000 0.040 5 170715913 intron variant C/G;T snv 0.21 2
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs33980500
TRAF3IP2-AS1 ; TRAF3IP2
0.742 0.200 6 111592059 missense variant C/T snv 8.6E-02 9.7E-02 14
rs206936
RPS10-NUDT3 ; NUDT3
0.882 0.160 6 34335092 intron variant A/G snv 0.34 8
rs778899140
PDE10A
0.925 6 165450268 missense variant T/C snv 4.0E-06 5
rs875989839
PDE10A
1.000 6 165450242 missense variant C/G snv 3
rs1057519475
FOXC1
1.000 0.080 6 1610761 stop gained C/T snv 2
rs372857241
FOXC1
1.000 0.080 6 1610586 stop gained C/G;T snv 1.8E-05 2
rs539815495
PRKN
6 161973365 missense variant A/G snv 1.1E-04 1.4E-05 1
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs2110267
DPP6
1.000 0.040 7 153838604 intergenic variant C/G snv 0.32 3
rs1057518644
HGSNAT
0.925 0.120 8 43192413 stop gained C/T snv 10
rs771138120
CDKN2A
0.827 0.120 9 21971191 missense variant G/A;C;T snv 9.1E-06; 4.5E-06 13
rs2281997
ENHO
0.882 0.240 9 34521869 intron variant T/A;C snv 5
rs1060504185
CDKN2A
9 21971116 missense variant G/A;C snv 1
rs914655
C9orf92
9 16208133 intron variant G/T snv 1.6E-02 1
rs1800544
ADRA2A
0.790 0.160 10 111076745 upstream gene variant G/C snv 0.59 12
rs121909731
GLUD1
0.851 0.120 10 87057692 missense variant G/A;C snv 4.0E-06 7
rs1057519866
NT5C2
0.851 0.120 10 103093198 missense variant C/T snv 5
rs1800035
ADRA2A
0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4
rs12765063
CUL2 ; CREM
10 35127641 intron variant G/A snv 0.14 2