Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1039002
PDE10A
0.851 0.080 6 165741969 intron variant G/A;T snv 5
rs1249144069
PITRM1-AS1 ; PITRM1
0.925 0.200 10 3165320 missense variant C/T snv 1.4E-05 5
rs1555910162
SHANK3
0.925 0.080 22 50721469 frameshift variant -/C delins 5
rs2958182
TCF4-AS1 ; TCF4
0.882 0.040 18 55481790 intron variant A/T snv 0.72 5
rs12201676 0.925 0.040 6 89022382 regulatory region variant T/C snv 0.21 4
rs12807809 0.882 0.160 11 124736389 upstream gene variant T/C snv 0.20 4
rs17746001 0.925 0.040 4 179734472 intergenic variant C/T snv 5.3E-02 4
rs2514218 0.925 0.040 11 113522272 regulatory region variant C/T snv 0.26 4
rs3916965 0.882 0.040 13 105451011 intergenic variant C/T snv 0.31 4
rs2070106
CNP
0.925 0.160 17 41973846 synonymous variant G/A snv 0.31 0.25 4
rs802568
CNTNAP2
0.925 0.040 7 146262151 intron variant T/G snv 0.17 4
rs947267
DAOA-AS1 ; DAOA
0.882 0.040 13 105487313 intron variant T/G snv 0.51 4
rs3738401
DISC1 ; TSNAX-DISC1
0.882 0.080 1 231694549 missense variant G/A snv 0.30 0.26 4
rs4436578
DRD2
0.925 0.080 11 113436043 intron variant C/T snv 0.73 4
rs2619538
DTNBP1
0.882 0.040 6 15664978 upstream gene variant A/T snv 0.54 4
rs104894685
FTL
0.925 0.120 19 48966317 missense variant G/A snv 4.0E-06 1.4E-05 4
rs12836771
HTR2C ; MIR1912 ; MIR1264
0.882 0.080 X 114650913 intron variant A/G snv 0.12 4
rs2054399
KCNMB2-AS1 ; KCNMB2
0.925 0.040 3 178623794 intron variant G/A;C snv 4
rs165940
LOC107986348 ; PDE4D
0.925 0.040 5 59383658 intron variant A/T snv 0.38 4
rs2857766
MOG
0.882 0.120 6 29666226 missense variant G/C snv 0.22 0.19 4
rs13211507
PGBD1
0.882 0.200 6 28289600 intron variant T/C snv 6.4E-02 4
rs4356203
PIK3C2A
0.925 0.040 11 17138601 intron variant A/G snv 0.31 4
rs701428
RTN4R
1.000 0.040 22 20241019 downstream gene variant A/G snv 0.56 4
rs7872515
SPTLC1
0.925 0.040 9 92060258 intron variant G/A snv 0.25 4
rs17110747
TPH2
0.882 0.120 12 72032174 3 prime UTR variant G/A snv 0.12 4