Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112543062
GNPTAB
0.851 0.280 12 101770161 missense variant T/C;G snv 1.2E-05 6
rs1060499679
GNPTAB
0.851 0.280 12 101770496 inframe deletion GTG/- delins 5
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6
rs1561515242
CAMK4
1.000 0.080 5 111482938 splice donor variant G/A snv 6
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs6277
DRD2
0.689 0.480 11 113412737 synonymous variant G/A snv 0.41 0.38 36
rs1801028
DRD2
0.716 0.200 11 113412762 missense variant G/C snv 2.7E-02 1.8E-02 24
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs1554776954
STXBP1
1.000 9 127661133 frameshift variant A/- delins 5
rs28939688
OPTN
0.807 0.040 10 13109270 missense variant G/A snv 7
rs1555103646
GRIN2B
1.000 0.040 12 13569964 missense variant C/A snv 4
rs1555103652
GRIN2B
0.882 0.240 12 13569973 missense variant A/C snv 11
rs2074898
NDUFS7
1.000 0.040 19 1391362 intron variant A/C;G snv 3
rs886041097
NAA15
0.882 0.160 4 139386152 stop gained C/G snv 9
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs40184
SLC6A3
0.851 0.120 5 1394962 intron variant C/T snv 0.45 5
rs41423247
NR3C1
0.695 0.440 5 143399010 intron variant G/C snv 0.31 23
rs550659379
NR3C1
0.882 0.160 5 143399780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs375382379
NR3C1
0.882 0.160 5 143399792 missense variant T/C snv 4.0E-06 5