Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3813867
LOC107984284 ; CYP2E1
0.732 0.240 10 133526101 intron variant G/A;C snv 13
rs1799732
DRD2 ; LOC105369501
0.790 0.160 11 113475529 intron variant -/G delins 11
rs6271
DBH-AS1 ; DBH
1.000 0.040 9 133657152 missense variant C/T snv 4.6E-02 4.8E-02 5
rs1611131
DBH-AS1 ; DBH
0.925 0.080 9 133657065 splice region variant A/G snv 0.28; 4.0E-06 0.25 3
rs12773625
CTNNA3 ; LOC101928961
1.000 0.040 10 66919791 intron variant T/A snv 0.41 2
rs589249
LOC105378648 ; LOC107984941
1.000 0.040 1 36696751 intergenic variant A/G;T snv 2
rs10211550
MOB4 ; HSPE1-MOB4
1.000 0.040 2 197518575 intron variant G/T snv 0.37 2
rs3747802
ABCB1 ; RUNDC3B
1.000 0.040 7 87713270 5 prime UTR variant A/C;G snv 1
rs490460
BACE1 ; BACE1-AS
1.000 0.040 11 117293049 splice region variant C/A;T snv 0.74 1
rs76432012
FTCDNL1 ; LINC01877
1.000 0.040 2 199712044 intron variant T/C snv 4.0E-02 1
rs1815774
FXYD6 ; FXYD6-FXYD2
1.000 0.040 11 117860724 intron variant G/C;T snv 1
rs3168238
FXYD6 ; FXYD6-FXYD2
1.000 0.040 11 117838930 non coding transcript exon variant T/G snv 4.0E-02 1
rs4938445
FXYD6 ; FXYD6-FXYD2
1.000 0.040 11 117874288 intron variant G/A snv 0.33 1
rs4938446
FXYD6 ; FXYD6-FXYD2
1.000 0.040 11 117874334 intron variant T/A;C snv 1
rs4597906
LOC102723914 ; LINC02264
1.000 0.040 4 117837640 intron variant C/G;T snv 1
rs2031921
LOC107984284 ; CYP2E1
1.000 0.040 10 133526369 non coding transcript exon variant T/A;C snv 1
rs2031922
LOC107984284 ; CYP2E1
1.000 0.040 10 133526589 non coding transcript exon variant T/C snv 0.13 1
rs1700
MIR198 ; FSTL1 ; LOC100130701
1.000 0.040 3 120395790 3 prime UTR variant C/T snv 0.10 1
rs10503899
NRG1 ; NRG1-IT1
1.000 0.040 8 32089718 intron variant A/G snv 0.33 1
rs893703
RBP1 ; LOC100507291
1.000 0.040 3 139531807 intron variant A/G snv 0.15 1