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
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 262
rs4680
COMT ; MIR4761
0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365
BDNF-AS ; BDNF
0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799945
LOC108783645 ; HFE
0.452 0.760 6 26090951 missense variant C/G;T snv 0.11 0.10 226
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs6313
HTR2A
0.562 0.640 13 46895805 synonymous variant G/A snv 0.41 0.40 82
rs6280
DRD3
0.602 0.520 3 114171968 missense variant C/T snv 0.63 0.54 57
rs6314
HTR2A
0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs3135932
IL10RA
0.677 0.480 11 117993348 missense variant A/G snv 0.13 0.11 23
rs1625579
MIR137HG
0.763 0.160 1 98037378 intron variant G/T snv 0.78 14
rs2229113
IL10RA
0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs2710323
ITIH1
0.851 0.080 3 52781889 intron variant T/C snv 0.49 0.54 7
rs17693963 0.882 0.040 6 27742386 upstream gene variant A/C;G snv 5
rs221774 0.851 0.080 7 100701361 upstream gene variant A/G;T snv 4
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs13001243 0.882 0.040 2 234306004 regulatory region variant G/A snv 7.5E-02 3
rs201048567 0.882 0.040 7 125615031 intergenic variant CA/- delins 1.0E-05 3
rs2997119 0.882 0.040 13 55819766 intergenic variant A/G snv 0.52 3
rs56196471 0.882 0.040 4 178642661 intergenic variant G/A snv 2.9E-02 3
rs62482377 0.882 0.040 7 156250946 intergenic variant G/C snv 0.10 3
rs7766730 0.882 0.040 6 65987110 intergenic variant C/A;T snv 3
rs77867520 0.882 0.040 4 11186225 intergenic variant C/T snv 7.2E-02 3
rs9354352 0.882 0.040 6 65986379 intergenic variant T/C snv 0.42 3