Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs2230345
GRK5
0.807 0.160 10 119326585 missense variant A/T snv 3.8E-02 9.0E-02 6
rs3208305
LPL
1.000 0.080 8 19966137 3 prime UTR variant A/T snv 0.36 4
rs386747134
CALHM1
0.882 0.120 10 103458495 missense variant AGC/GGT mnv 3
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs3865444
CD33
0.851 0.160 19 51224706 upstream gene variant C/A snv 0.25 8
rs3735964
LPL
1.000 0.080 8 19966534 3 prime UTR variant C/A snv 9.1E-02 5
rs1799999
PPP1R3A
0.882 0.160 7 113878379 missense variant C/A snv 0.22 0.17 4
rs890293
CYP2J2
0.851 0.200 1 59926822 upstream gene variant C/A snv 8.6E-02 4
rs2373115
GAB2
0.925 0.080 11 78380104 intron variant C/A snv 0.24 2
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs6084
LIPC
0.925 0.120 15 58545839 synonymous variant C/A;G snv 1.2E-05; 0.43 2
rs6665
MME
1.000 0.080 3 155183416 3 prime UTR variant C/A;G snv 1
rs266729
ADIPOQ
0.637 0.560 3 186841685 upstream gene variant C/A;G;T snv 37
rs498055 0.925 0.080 10 95595157 non coding transcript exon variant C/A;G;T snv 0.39 2
rs746682028
BDNF ; BDNF-AS
0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 36
rs75932628
LOC105375056 ; TREM2
0.662 0.480 6 41161514 missense variant C/A;T snv 6.8E-05; 2.6E-03 28
rs1035071612
MIR6886 ; LDLR
0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs1799986
LRP1
0.851 0.120 12 57141483 missense variant C/A;T snv 8.0E-06; 0.13 4
rs1476679
ZCWPW1
0.925 0.080 7 100406823 intron variant C/A;T snv 4.0E-06; 0.74 2
rs1562990
MS4A4A
0.925 0.080 11 60255614 intron variant C/A;T snv 2
rs600491
DHCR24
0.925 0.080 1 54867852 intron variant C/A;T snv 2
rs536360
SORL1
1.000 0.080 11 121457328 intron variant C/A;T snv 0.52 1
rs771608420
AKAP9
1.000 0.080 7 92001217 missense variant C/A;T snv 2.0E-05; 8.0E-06 1
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131