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
rs1801131
MTHFR
0.535 0.840 1 11794419 missense variant T/G snv 0.29 0.26 93
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs4846049
C1orf167 ; MTHFR
0.776 0.360 1 11790308 3 prime UTR variant T/A;G snv 11
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 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
rs2252865
RERE
0.851 0.040 1 8362616 intron variant T/C snv 0.72 6
rs595961
AGO1
0.807 0.160 1 35902179 intron variant A/G snv 0.30 0.37 6
rs6694545 0.851 0.040 1 29964421 intergenic variant A/G snv 0.58 5
rs1538979
TSNAX-DISC1 ; DISC1
0.882 0.160 1 231761122 intron variant C/T snv 0.19 3
rs2391769
LOC105378866
0.925 0.040 1 96513405 regulatory region variant A/G;T snv 3
rs10489744
RXRG
0.925 0.040 1 165411386 intron variant G/A snv 0.55 2
rs11162556 0.925 0.040 1 78795698 intergenic variant A/G snv 0.32 2
rs11210887
PTPRF
0.925 0.040 1 43610348 intron variant G/A snv 0.52 2
rs113551349
SLC6A9
0.925 0.040 1 44009451 intron variant C/T snv 0.20 2
rs2782639
PTPRF
0.925 0.040 1 43540668 intron variant A/G snv 0.26 2
rs3001723
PTPRF
0.925 0.040 1 43572014 intron variant G/A snv 0.40 2
rs56319043
KDM4A-AS1 ; ST3GAL3 ; KDM4A
0.925 0.040 1 43705540 intron variant C/T snv 0.17 2
rs10910623
MAP10
1.000 0.040 1 232802953 upstream gene variant G/A snv 7.5E-02 1
rs11122330
DISC1 ; TSNAX-DISC1
1.000 0.040 1 231762845 intron variant A/G snv 0.14 1
rs112984125
ST3GAL3 ; KDM4A-AS1
1.000 0.040 1 43707752 intron variant G/A snv 0.25 1