Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13440581
GPR50
0.882 0.080 X 151181399 missense variant A/G snv 0.45 0.45 5
rs174697
ARVCF ; COMT
0.851 0.080 22 19966309 intron variant A/G snv 0.88 5
rs2028122
RORA ; RORA-AS1
0.851 0.120 15 60549076 intron variant A/G snv 0.51 4
rs561077
GPR50
0.882 0.080 X 151181177 missense variant A/G snv 0.43 0.45 4
rs1187329
NTRK2
0.925 0.080 9 84674365 intron variant A/G snv 0.52 3
rs1045642
ABCB1
0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs11932595
CLOCK
0.827 0.160 4 55457430 intron variant A/G;T snv 12
rs786204858
PTEN
0.776 0.280 10 87933079 missense variant A/G;T snv 11
rs112025902 0.925 0.080 4 120232669 intron variant A/G;T snv 4
rs1858232
NOS1AP
0.882 0.080 1 162334048 intron variant A/G;T snv 4
rs2910709
GDNF-AS1
0.882 0.120 5 37811762 non coding transcript exon variant A/G;T snv 4
rs11030101
BDNF-AS ; BDNF
0.763 0.160 11 27659197 5 prime UTR variant A/T snv 0.36 10
rs1922242
ABCB1
0.827 0.120 7 87544351 intron variant A/T snv 0.43 8
rs1131691771
PHIP ; IRAK1BP1
0.807 0.160 6 78958469 splice donor variant ACTT/- delins 18
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs324420
FAAH
0.637 0.440 1 46405089 missense variant C/A snv 0.24 0.26 48
rs3800373
LOC101929309 ; FKBP5
0.752 0.200 6 35574699 3 prime UTR variant C/A snv 0.68 22
rs1057523354
COL4A1
0.763 0.480 13 110179387 missense variant C/A snv 13
rs1130214
AKT1
0.742 0.280 14 104793397 5 prime UTR variant C/A snv 0.31 12
rs2283265
DRD2
0.776 0.160 11 113414814 intron variant C/A snv 0.16 12
rs1800044
HTR1A
0.827 0.200 5 63961061 missense variant C/A snv 3.7E-03 3.8E-03 8
rs2740210
OXT ; LOC101929098
0.827 0.120 20 3072609 downstream gene variant C/A snv 0.28 7
rs766020740
MIR4761 ; COMT
0.851 0.120 22 19963644 missense variant C/A snv 4.0E-06 5
rs78162420
TPH2
0.882 0.120 12 71941600 missense variant C/A snv 2.1E-03 7.1E-04 4