Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3851179 0.752 0.280 11 86157598 downstream gene variant T/C snv 0.70 15
rs12273363
BDNF
0.807 0.120 11 27723312 intron variant T/C snv 0.16 11
rs104886033
DHCR7
0.827 0.160 11 71444952 start lost T/C snv 1.2E-05; 4.0E-06 3.5E-05 10
rs10748842
NRG3
0.807 0.120 10 81889983 intron variant T/C snv 0.13 8
rs63749806
PSEN1
0.827 0.080 14 73186902 missense variant T/C snv 7
rs747105516
PSPH
0.851 0.120 7 56015139 missense variant T/C snv 4.0E-06 5
rs12752888
LINC02784
0.851 0.160 1 54527266 downstream gene variant T/C snv 0.26 4
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs2731880 0.925 0.040 5 36603282 upstream gene variant T/C snv 0.52 3
rs3875089
AQP4 ; AQP4-AS1
0.925 0.080 18 26865469 intron variant T/C snv 0.19 3
rs1245342105
SPTBN1
1.000 0.040 2 54622367 missense variant T/C snv 4.0E-06 2
rs17090219 0.925 0.080 18 56523802 intergenic variant T/C snv 7.4E-02 2
rs2283368
KL
1.000 0.040 13 33019132 intron variant T/C snv 0.15 2
rs2303579
NEDD4
0.925 0.040 15 55860531 missense variant T/C snv 0.74 0.72 2
rs3936289
ST6GAL1
0.925 0.080 3 187037169 intron variant T/C snv 0.33 2
rs1041536 1.000 0.040 20 9907627 intergenic variant T/C snv 0.46 1
rs113793030 1.000 0.040 10 70287104 upstream gene variant T/C snv 1.7E-02 1
rs115764752
LOC105371614
1.000 0.040 1 171778066 upstream gene variant T/C snv 7.9E-03 1
rs116237496 1.000 0.040 8 101033687 upstream gene variant T/C snv 4.0E-02 1
rs1216578110
APP
1.000 0.040 21 25955652 missense variant T/C snv 4.0E-06 7.0E-06 1
rs12624302
LOC107985840
1.000 0.040 2 3168181 regulatory region variant T/C snv 3.0E-02 1
rs13447287
CDC45
1.000 0.040 22 19518601 intron variant T/C snv 6.9E-03 1
rs139660738 1.000 0.040 12 94791412 intergenic variant T/C snv 6.3E-03 1
rs148992089
EBF1
1.000 0.040 5 158952834 intron variant T/C snv 6.1E-03 1
rs150759334 1.000 0.040 4 60800528 downstream gene variant T/C snv 9.4E-03 1