Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs12682807
SLC1A1 ; SPATA6L
1.000 0.040 9 4574022 splice region variant A/C snv 0.11 8.5E-02 1
rs11583978
DLGAP3
0.925 0.040 1 34864921 downstream gene variant A/C;G snv 2
rs4401971 1.000 0.040 9 11890045 intron variant A/C;G;T snv 1
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1799971
OPRM1
0.559 0.600 6 154039662 missense variant A/G snv 0.19 0.12 95
rs11174202
TAFA2
0.925 0.040 12 61858476 intron variant A/G snv 0.49 2
rs762178
OLIG2
0.925 0.040 21 33027093 synonymous variant A/G snv 0.51 0.53 2
rs1265692223
HTR3E ; LOC105374249 ; HTR3E-AS1
1.000 0.040 3 184100530 missense variant A/G snv 4.0E-06 1
rs2364841
ADCK1
1.000 0.040 14 77817693 intron variant A/G snv 0.86 1
rs28696717 1.000 0.040 1 153493087 intergenic variant A/G snv 0.18 1
rs3785817
GRN
1.000 0.040 17 44346297 intron variant A/G snv 0.28 1
rs56151798
TPH1
1.000 0.040 11 18022863 synonymous variant A/G snv 6.0E-03 6.4E-03 1
rs6131293 1.000 0.040 20 12014779 intergenic variant A/G snv 0.79 1
rs8190748
GAD2
1.000 0.040 10 26280826 intron variant A/G snv 0.44 1
rs12635725 1.000 0.040 3 1895465 intergenic variant A/G;T snv 1
rs297941
LINC02395
1.000 0.040 12 49925303 non coding transcript exon variant A/G;T snv 1
rs6662980
DLGAP3
1.000 0.040 1 34894477 intron variant A/G;T snv 1
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 18
rs1755715
GPR135
1.000 0.040 14 59440374 intron variant A/T snv 0.55 1
rs6109227 1.000 0.040 20 12018497 intergenic variant A/T snv 0.79 1
rs1059004
OLIG2
0.925 0.040 21 33028155 3 prime UTR variant C/A snv 0.41 4
rs3747767
LOC112267857
1.000 0.040 6 79547564 intergenic variant C/A snv 8.2E-02 2
rs1000592 1.000 0.040 2 118939624 upstream gene variant C/A snv 6.4E-03 1
rs4565946
TPH2
0.827 0.080 12 71942989 intron variant C/A;G;T snv 7