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
rs699
AGT
0.501 0.800 1 230710048 missense variant A/G snv 0.55 0.58 134
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
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
rs1194897557
MTHFR
0.827 0.240 1 11796276 missense variant A/G snv 8.0E-06 7
rs4650608 0.851 0.040 1 78772330 intergenic variant T/C snv 0.29 7
rs6675281
DISC2 ; DISC1 ; TSNAX-DISC1 ; LOC105373170
0.827 0.080 1 231818355 missense variant C/T snv 0.11 0.14 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
rs2812393
TSNAX-DISC1 ; DISC1
0.807 0.080 1 231777927 intron variant G/C snv 0.61 6
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
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
rs115777110
LOC107985255
0.882 0.040 1 208936211 intergenic variant T/C snv 1.2E-02 3
rs146330533
ARHGEF10L
0.882 0.040 1 17669971 intron variant G/A snv 1.2E-02 3
rs1541187
BCL9
0.882 0.040 1 147579693 intron variant C/G;T snv 3
rs6703335
SDCCAG8
0.882 0.040 1 243445665 intron variant A/G snv 0.50 3
rs821577
DISC1 ; TSNAX-DISC1 ; DISC1-IT1
0.882 0.160 1 231931311 intron variant T/C;G snv 3