Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs80358259
NPC1
0.851 0.320 18 23536736 missense variant A/G snv 2.0E-04 2.4E-04 9
rs4795541
SLC6A4 ; LOC105371720
0.807 0.200 17 30237299 upstream gene variant A/G snv 7
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs145606134
RAB40AL ; LINC00630
0.882 0.240 X 102937494 missense variant A/G snv 5.4E-03 4.1E-03 5
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs80356734
TARDBP
0.851 0.160 1 11022464 missense variant A/G snv 4
rs11030108
BDNF ; BDNF-AS
1.000 0.040 11 27673917 intron variant A/G snv 0.72 3
rs1372439127
GRN
0.925 0.080 17 44352420 missense variant A/G snv 4.0E-06 3
rs1938526
ANK3
0.882 0.040 10 60540625 intron variant A/G snv 8.3E-02 3
rs2344484 0.925 0.040 5 135540941 upstream gene variant A/G snv 0.47 3
rs55781031
BCHE
0.925 0.080 3 165786432 intron variant A/G snv 5.3E-02 3
rs690016544
STUB1 ; JMJD8 ; LINC02867
0.882 0.160 16 681186 missense variant A/G snv 4.8E-06 3
rs6910730
TREM1
0.925 0.080 6 41278895 intron variant A/G snv 0.21 3
rs10521467
PCSK5
0.925 0.080 9 76036575 intron variant A/G snv 0.12 2
rs1157659 1.000 0.040 11 27736075 intron variant A/G snv 0.37 2
rs9526984
KL
1.000 0.040 13 33035800 intron variant A/G snv 5.5E-02 2
rs116065238 1.000 0.040 1 171482283 upstream gene variant A/G snv 4.3E-03 1
rs12435940 1.000 0.040 14 25552779 intergenic variant A/G snv 0.97 1
rs138901640 1.000 0.040 9 118031487 intron variant A/G snv 5.5E-03 1
rs140564516
LASP1
1.000 0.040 17 38873719 intron variant A/G snv 8.7E-03 1
rs141990949
CFAP299
1.000 0.040 4 80443266 intron variant A/G snv 1.2E-02 1
rs142609537 1.000 0.040 15 95675665 intron variant A/G snv 1.8E-02 1
rs147368169
TSNARE1
1.000 0.040 8 142389482 intron variant A/G snv 1.1E-02 1
rs1955873 1.000 0.040 14 25573788 intergenic variant A/G snv 0.97 1
rs2077823
LRRTM4
1.000 0.040 2 77021786 intron variant A/G snv 0.12 1