Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2227631
SERPINE1
0.742 0.200 7 101126257 upstream gene variant A/G snv 0.54 13
rs1799889
SERPINE1
0.649 0.600 7 101126430 upstream gene variant A/G snv 31
rs696217
GHRL ; GHRLOS
0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 32
rs553040076
CDC37 ; PDE4A
0.925 0.080 19 10417700 missense variant T/A snv 4.5E-05 7.7E-05 3
rs156243 0.925 0.080 6 104416939 intergenic variant G/A snv 0.65 6
rs3916966 0.882 0.080 13 105458546 upstream gene variant C/A snv 0.63 4
rs1935062
DAOA ; DAOA-AS1
0.882 0.080 13 105475787 intron variant A/C snv 0.32 3
rs1013940
SLC5A7
0.827 0.160 2 107992192 missense variant A/G snv 9.3E-02 7.4E-02 6
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs1800035
ADRA2A
0.925 0.080 10 111078794 missense variant C/G;T snv 1.9E-03 4
rs1800587
IL1A
0.620 0.720 2 112785383 upstream gene variant G/A;C snv 0.32 43
rs16944
IL1B
0.531 0.920 2 112837290 upstream gene variant A/G snv 0.57 92
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs1176744
HTR3B
0.708 0.240 11 113932306 missense variant A/C snv 0.33 0.36 19
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6318
HTR2C ; LOC105373313
0.623 0.520 X 114731326 missense variant C/G;T snv 42
rs10223646
DSE
0.882 0.080 6 116296236 intron variant C/T snv 0.41 4
rs3782218
NOS1
0.882 0.120 12 117333706 intron variant C/T snv 0.19 5
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1801133
MTHFR
0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs10510057 0.925 0.080 10 119551536 intergenic variant G/C snv 0.22 3