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
rs1805087
MTR
0.496 0.800 1 236885200 missense variant A/G snv 0.20 0.21 135
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
rs821616
DISC1 ; TSNAX-DISC1
0.752 0.200 1 232008852 missense variant A/T snv 0.26 0.29 13
rs6691840
GRIK3
0.827 0.120 1 36859876 missense variant A/C;G snv 0.27; 9.2E-05 5
rs10494251
BCL9
0.851 0.040 1 147552120 intron variant C/T snv 5.8E-02 4
rs6586354 0.851 0.040 1 234897489 intron variant G/A snv 0.25 4
rs672607
BCL9
0.851 0.040 1 147581540 intron variant G/A snv 0.12 4
rs688325
BCL9
0.851 0.040 1 147605490 intron variant G/A snv 0.19 4
rs111365677 0.925 0.040 1 99463578 upstream gene variant T/C snv 2.3E-03 3
rs1541187
BCL9
0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs2984618
TAL1
0.925 0.040 1 47224766 intron variant G/T snv 0.52 3
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs55679149
LOC105378841
0.925 0.040 1 89068655 upstream gene variant C/T snv 0.34 3
rs7555693 0.925 0.040 1 106295917 intergenic variant G/A snv 0.45 3
rs760161369
MTHFR
0.882 0.040 1 11800214 missense variant G/A;C snv 2.8E-05; 4.0E-06 3
rs946903
BCL9
0.882 0.040 1 147625465 3 prime UTR variant T/C snv 0.25 3
rs782212
LOC105378797
0.925 0.040 1 72479983 intron variant C/T snv 0.34 2
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs1344706
ZNF804A
0.701 0.160 2 184913701 intron variant A/C;T snv 21
rs2253206 0.851 0.080 2 207527254 intron variant A/G snv 0.47 6
rs11904814
CREB1
0.851 0.080 2 207562074 intron variant T/G snv 0.30 5
rs231779
CTLA4
0.827 0.160 2 203869764 intron variant C/T snv 0.41 5