Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs6296
HTR1B ; LOC105377864
0.732 0.160 6 77462543 synonymous variant C/G snv 0.31 0.27 23
rs17689918
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.851 0.080 17 45832722 intron variant G/A snv 0.15 6
rs1042778
CAV3 ; OXTR
0.925 0.040 3 8752859 3 prime UTR variant G/A;C;T snv 3
rs536599 1.000 0.080 4 46196917 intergenic variant G/T snv 0.47 2
rs7632287
CAV3
1.000 0.040 3 8749760 intron variant G/A snv 0.32 2
rs2119183
GABRA2
1.000 0.080 4 46270789 intron variant G/A snv 7.6E-02 2
rs3756007
GABRA2
1.000 0.080 4 46389047 5 prime UTR variant T/C snv 5.4E-02 2
rs11941860
GABRG1
1.000 0.080 4 46080161 intron variant C/T snv 0.12 2
rs12106331 21 37354975 intron variant A/G snv 0.17 1
rs2835702 21 37352009 intron variant T/C snv 0.17 1
rs346425 5 63300417 upstream gene variant T/C snv 0.48 1
rs4714329 6 40305718 intergenic variant G/A snv 0.57 1
rs9471290 6 40292776 intergenic variant G/A snv 0.38 1
rs11215217
LOC105369506
11 114818979 intergenic variant C/T snv 6.8E-02 1
rs4564970
OXTR ; CAV3
3 8768722 intron variant G/A;C snv 1