Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1060503383
SYNGAP1
0.882 0.200 6 33441318 stop gained C/T snv 14
rs6994992
NRG1
0.790 0.120 8 31638065 upstream gene variant C/A;T snv 13
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 12
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
rs80338758
MED12
0.790 0.400 X 71127367 missense variant C/A;T snv 12
rs1555103652
GRIN2B
0.882 0.240 12 13569973 missense variant A/C snv 11
rs27072
SLC6A3
0.807 0.120 5 1394407 3 prime UTR variant C/A;T snv 11
rs121917893
NLGN3
0.807 0.160 X 71167508 missense variant C/T snv 10
rs2066713
SLC6A4
0.807 0.200 17 30224647 intron variant G/A snv 0.34 9
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 9
rs886041097
NAA15
0.882 0.160 4 139386152 stop gained C/G snv 9
rs1126647
CXCL8
0.827 0.160 4 73743328 3 prime UTR variant A/T snv 0.31 8
rs2069845
IL6
0.807 0.120 7 22730530 intron variant G/A snv 0.61 8
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs28939688
OPTN
0.807 0.040 10 13109270 missense variant G/A snv 7
rs4251417
SLC6A4
0.827 0.200 17 30224840 intron variant C/T snv 6.8E-02 7
rs7224199
SLC6A4
0.827 0.160 17 30196708 3 prime UTR variant G/T snv 0.49 7
rs80359636
BRCA2
0.851 0.240 13 32354921 frameshift variant CT/- delins 2.8E-05 7
rs1018381
DTNBP1
0.882 0.040 6 15656839 intron variant G/A snv 0.16 6
rs1224426272
CIT
0.925 0.040 12 119869138 missense variant C/T snv 6
rs13438494
PCLO
1.000 0.040 7 82759398 intron variant T/G snv 0.61 6
rs1561515242
CAMK4
1.000 0.080 5 111482938 splice donor variant G/A snv 6
rs5177
LRP8
0.851 0.120 1 53246063 3 prime UTR variant G/A;C snv 6
rs7341475
RELN
0.851 0.240 7 103764368 intron variant G/A snv 0.17 6