Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3749034
GAD1
0.827 0.040 2 170816965 5 prime UTR variant G/A;T snv 6
rs11178997
TPH2
0.827 0.040 12 71938373 upstream gene variant T/A snv 0.12 5
rs9804190
ANK3
0.882 0.040 10 60080073 intron variant C/T snv 0.30 5
rs1876831
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.925 0.040 17 45830379 non coding transcript exon variant C/G;T snv 4.4E-06; 0.14 4
rs495225
GHSR
0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 4
rs12944712
CRHR1 ; LINC02210-CRHR1
0.925 0.040 17 45793781 intron variant G/A snv 0.35 3
rs16965628
SLC6A4
0.882 0.040 17 30228407 intron variant G/C snv 0.14 3
rs2400707
ADRB2
1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 3
rs10055255
CRHBP
1.000 0.040 5 76968168 intron variant A/T snv 0.50 2
rs1042357
ALOX12 ; ALOX12-AS1
0.925 0.040 17 7001742 synonymous variant T/C;G snv 0.59 2
rs1799923
CCK
0.925 0.040 3 42264802 5 prime UTR variant A/G snv 0.82 2
rs4775301
RORA
0.925 0.040 15 60834660 intron variant T/C;G snv 2
rs56242606
VWDE
1.000 0.040 7 12382283 intron variant T/C snv 5.3E-02 2
rs6470292
LOC105375743 ; LINC00964
1.000 0.040 8 124855801 intron variant A/G snv 0.17 2
rs683250
LOC107984425 ; DLG2
1.000 0.040 11 83565125 intron variant A/G;T snv 2
rs7208505
SKA2
1.000 0.040 17 59110368 3 prime UTR variant G/A;C;T snv 2
rs8024133
RORA
0.925 0.040 15 60838440 intron variant C/T snv 0.42 2
rs8041061
RORA
0.925 0.040 15 60832639 intron variant G/T snv 0.39 2
rs10144436
DICER1
1.000 0.040 14 95090065 3 prime UTR variant C/A snv 2.9E-02 1
rs10170218 1.000 0.040 2 187949717 intron variant A/C snv 0.25 1
rs1033962
PRTFDC1
1.000 0.040 10 24927877 intron variant C/T snv 0.33 1
rs10744891
NOS1
1.000 0.040 12 117284536 intron variant G/T snv 0.41 1
rs10852889
ALOX12 ; ALOX12-AS1
1.000 0.040 17 6997526 intron variant C/A;G;T snv 1
rs11599164
ANK3
1.000 0.040 10 60072226 missense variant G/T snv 7.2E-02 7.3E-02 1
rs1187327
NTRK2
1.000 0.040 9 84673625 intron variant T/C snv 0.50 1