Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs1805054
HTR6
0.708 0.200 1 19666020 synonymous variant C/T snv 0.15; 8.0E-06 0.16 17
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs1200746244
MTHFR
0.807 0.080 1 11801287 missense variant C/T snv 4.0E-06 7.0E-06 11
rs2271933
HCRTR1
0.807 0.080 1 31626924 missense variant A/G snv 0.56 0.50 9
rs3093077 0.827 0.200 1 159709846 upstream gene variant A/C;G;T snv 9
rs2568958
LOC105378797
0.882 0.160 1 72299433 intron variant G/A;C snv 8
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs766288
TSNAX-DISC1 ; TSNAX
0.790 0.080 1 231557942 intron variant G/T snv 0.40 7
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs301806
RERE
0.851 0.120 1 8422018 intron variant C/T snv 0.62 6
rs4648308
PTGS2
0.851 0.160 1 186671485 downstream gene variant C/T snv 0.27 5
rs6691840
GRIK3
0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs2094081
RHBDL2
0.925 0.080 1 38927359 intron variant G/A;C snv 4
rs301807
RERE-AS1 ; RERE
0.925 0.080 1 8424763 intron variant A/G;T snv 4
rs3738401
DISC1 ; TSNAX-DISC1
0.882 0.080 1 231694549 missense variant G/A snv 0.30 0.26 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4