Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 10
rs6269
COMT ; MIR4761
0.827 0.240 22 19962429 5 prime UTR variant A/G snv 0.38 10
rs1834306
MIR10526 ; MIR100 ; MIR100HG
0.776 0.200 11 122152479 intron variant A/G snv 0.49 9
rs61748421
MECP2
0.807 0.200 X 154031326 stop gained G/A;T snv 9
rs1057518946
GJB1
0.882 0.080 X 71223816 missense variant G/T snv 8
rs3813034
SLC6A4
0.827 0.160 17 30197786 3 prime UTR variant A/C snv 0.40 8
rs6276
DRD2
0.807 0.320 11 113410675 3 prime UTR variant C/T snv 0.54 8
rs1536309
MIR146B
0.851 0.160 10 102435445 upstream gene variant A/G snv 0.32 7
rs1800610
TNF
0.807 0.320 6 31576050 intron variant G/A snv 8.4E-02 7
rs2295633
FAAH
0.827 0.120 1 46408711 intron variant A/G;T snv 7
rs6801957
SCN10A
1.000 0.080 3 38725824 intron variant T/C snv 0.67 7
rs10877969
AVPR1A
0.882 0.120 12 63153459 intron variant T/C snv 0.26 6
rs8007267 0.882 0.200 14 54912273 intergenic variant C/T snv 0.31 6
rs2053044
ADRB2
1.000 0.040 5 148825809 5 prime UTR variant A/G snv 0.59 5
rs796590326
P2RX7 ; LOC105370032
0.851 0.200 12 121162449 missense variant GT/AC mnv 5
rs10166942
TRPM8
0.925 0.040 2 233916448 upstream gene variant T/C snv 0.40 4
rs1057518927
OAT
0.925 0.080 10 124402952 missense variant T/C snv 4
rs61751364
MECP2
0.882 0.120 X 154030944 frameshift variant CGGAT/- delins 4
rs80338761
SEPTIN9
0.882 0.080 17 77402298 missense variant C/T snv 4
rs8136867
MAPK1
0.882 0.080 22 21850504 intron variant G/A snv 0.55 4
rs10483639 1.000 0.040 14 54839739 downstream gene variant G/C snv 0.26 3
rs16868943
COL11A2
1.000 0.040 6 33179950 intron variant G/A snv 2.9E-02 3
rs17197936 0.925 0.040 13 37601702 upstream gene variant T/C snv 5.2E-02 3
rs2206593
PTGS2
0.925 0.080 1 186673297 3 prime UTR variant A/G snv 0.95 3
rs2233409
NFKBIA
1.000 0.080 14 35405064 upstream gene variant G/A snv 0.19 3