Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs242941
MAPT-AS1 ; CRHR1 ; LINC02210-CRHR1
0.790 0.200 17 45815154 intron variant A/C snv 0.62 9
rs11142387 9 70383416 downstream gene variant A/C snv 0.49 7
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs2074898
NDUFS7
1.000 0.040 19 1391362 intron variant A/C;G snv 3
rs4916723
LINC00461
0.925 0.040 5 88558577 intron variant A/C;G;T snv 4
rs2509843 11 98254676 intergenic variant A/C;G;T snv 2
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2049161
DLGAP1
18 4127583 intron variant A/C;T snv 0.22 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1800871
IL19 ; IL10
0.508 0.800 1 206773289 5 prime UTR variant A/G snv 0.69 108
rs9340799
ESR1
0.583 0.680 6 151842246 intron variant A/G snv 0.32 62
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs9296158
FKBP5 ; LOC112267956
0.763 0.080 6 35599305 intron variant A/G snv 0.65 16
rs2229113
IL10RA
0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs736707
LOC101927870 ; RELN
0.851 0.040 7 103489956 intron variant A/G snv 0.30 6
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs11740562
ADAM19
5 157515277 intron variant A/G snv 7.1E-02 2
rs12745968
DIPK1A
1 92936280 intron variant A/G snv 0.36 2
rs771065515
LMNA
1 156115240 missense variant A/G snv 2.5E-05 7.0E-06 2
rs374926367
LMNA
1 156139089 missense variant A/G snv 1.2E-04 1.0E-04 1
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs2710102
CNTNAP2
0.790 0.120 7 147877298 intron variant A/G;T snv 12
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