Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9983925
ADARB1
21 45216929 intron variant C/T snv 0.46 4
rs1799920
HTR1A
5 63961656 missense variant C/G;T snv 3.2E-04 2
rs1799921
HTR1A
5 63961638 missense variant T/C snv 9.4E-03 9.3E-03 2
rs200754713
PSEN2
1 226888954 missense variant A/G snv 4.0E-06; 4.0E-06 2
rs2049161
DLGAP1
18 4127583 intron variant A/C;T snv 0.22 2
rs279827
GABRA2
4 46332685 splice region variant A/G;T snv 0.44 0.41 2
rs35369693
AVPR1B
1 206116696 missense variant C/G;T snv 4.3E-02 2
rs1466835565
HK1
10 69368539 missense variant A/G snv 1
rs754747375
HK1
10 69369252 missense variant A/G snv 8.0E-06 7.0E-06 1
rs2535629
ITIH3
0.827 0.040 3 52799203 intron variant G/A;C snv 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
rs28939688
OPTN
0.807 0.040 10 13109270 missense variant G/A snv 6
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs945032
BDKRB2
0.882 0.040 14 96204324 upstream gene variant T/C snv 0.78 5
rs9804190
ANK3
0.882 0.040 10 60080073 intron variant C/T snv 0.30 5
rs1059004
OLIG2
0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 4
rs1133503
MANEA
1.000 0.040 6 95606712 3 prime UTR variant C/G;T snv 4
rs2074898
NDUFS7
1.000 0.040 19 1391362 intron variant A/C;G snv 3
rs2400707
ADRB2
1.000 0.040 5 148825489 5 prime UTR variant A/G;T snv 3
rs3915512
DLG1 ; MIR4797
1.000 0.040 3 197295369 intron variant A/G;T snv 3
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 2
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs9470080
FKBP5
0.827 0.080 6 35678658 intron variant T/A;C snv 13