Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1085308056
PTEN
0.851 0.160 10 87957850 splice region variant C/G snv 8
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs1922242
ABCB1
0.827 0.120 7 87544351 intron variant A/T snv 0.43 8
rs900418273
ANKK1
0.807 0.120 11 113393764 missense variant A/G snv 8
rs1202184
ABCB1
0.851 0.120 7 87584585 intron variant C/T snv 0.39 7
rs2072621
GPR50-AS1 ; GPR50
0.851 0.080 X 151177387 non coding transcript exon variant C/A;G snv 7
rs2740210
OXT ; LOC101929098
0.827 0.120 20 3072609 downstream gene variant C/A snv 0.28 7
rs387906653
SLC20A2
0.882 0.120 8 42428829 stop gained C/A;T snv 7
rs7194256
SLC6A2
0.827 0.120 16 55703779 3 prime UTR variant C/G;T snv 7
rs7766029 0.851 0.080 6 88137716 downstream gene variant T/C snv 0.51 7
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs12938031
LINC02210-CRHR1
0.851 0.160 17 45777136 intron variant A/G snv 0.26 6
rs17689918
LINC02210-CRHR1 ; MAPT-AS1 ; CRHR1
0.851 0.080 17 45832722 intron variant G/A snv 0.15 6
rs1843809
TPH2
0.851 0.080 12 71954918 intron variant G/T snv 0.77 6
rs2349775
NXPH1
0.851 0.120 7 8678450 intron variant G/A;C snv 6
rs41305272
MAP2K5
0.851 0.120 15 67807105 3 prime UTR variant C/T snv 2.4E-02 6
rs10501320
MADD ; MADD-AS1
0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 5
rs11111
GDNF-AS1 ; GDNF
0.882 0.080 5 37814000 3 prime UTR variant T/C snv 0.22 5
rs2070587
DAO
0.882 0.080 12 108883967 intron variant T/G snv 0.32 5
rs2072115
RAPGEF3
0.882 0.080 12 47751585 intron variant A/C;G snv 5
rs3096140
GDNF ; GDNF-AS1
0.882 0.080 5 37832731 intron variant G/A snv 0.69 5
rs7209436
LINC02210-CRHR1 ; CRHR1
0.851 0.200 17 45792776 intron variant C/T snv 0.43 5
rs75012854
MIR4761 ; COMT
0.882 0.200 22 19962641 missense variant A/G snv 7.0E-06 5
rs8067056
MAPT
0.925 0.080 17 46006582 intron variant T/C;G snv 0.30 5
rs1057518806
HMBS
1.000 0.040 11 119093155 frameshift variant G/- del 4