Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs26318
COMMD10
0.925 0.040 5 116352208 intron variant C/T snv 0.99 3
rs324899
LINC00461
0.925 0.040 5 88619764 intron variant A/G snv 0.97 2
rs914715
TLE4
1.000 0.040 9 79695983 intron variant T/A snv 0.96 1
rs10198175 0.925 0.080 2 20934123 intergenic variant A/G snv 0.93 3
rs4947962
LOC105375284
1.000 0.040 7 55008114 intergenic variant G/C snv 0.93 1
rs3128296
PRKCZ
1.000 0.040 1 2137467 intron variant G/T snv 0.92 1
rs1534891
CSNK1E ; TPTEP2-CSNK1E
0.827 0.200 22 38299094 intron variant T/C snv 0.90 5
rs506597 0.882 0.040 7 100715797 upstream gene variant A/G snv 0.90 4
rs1521470
ADCY1
0.925 0.040 7 45607253 intron variant A/G snv 0.89 2
rs140504
LOC107985554 ; BCR
0.882 0.040 22 23285182 missense variant A/G snv 0.81 0.86 3
rs1516725
ETV5 ; DGKG
0.925 0.120 3 186106215 intron variant T/C snv 0.86 8
rs1012053
DGKH
1.000 0.040 13 42079301 intron variant C/A snv 0.85 1
rs2934442
CGNL1
1.000 0.040 15 57470595 intron variant C/T snv 0.84 1
rs6502097
SECTM1
0.882 0.040 17 82328303 5 prime UTR variant C/G snv 0.83 3
rs749909
TRPM2
1.000 0.040 21 44434924 intron variant G/A snv 0.83 1
rs548181
FEZ1 ; STT3A-AS1 ; STT3A
0.851 0.040 11 125591814 5 prime UTR variant A/G snv 0.83 5
rs6568686
TRAF3IP2-AS1
1.000 0.040 6 111551279 intron variant T/C snv 0.83 1
rs4765913
CACNA1C
1.000 0.040 12 2310730 intron variant A/T snv 0.82 1
rs7240206
LOC105372213
1.000 0.040 18 76723198 regulatory region variant C/G snv 0.82 1
rs534654
TMEM165
0.925 0.040 4 55424053 non coding transcript exon variant A/G snv 0.81 2
rs4774388
RORA
0.807 0.200 15 61174799 intron variant C/T snv 0.81 6
rs1611115
DBH
0.732 0.280 9 133635393 upstream gene variant T/C snv 0.80 16
rs4800149
CABLES1
0.882 0.040 18 23164290 intron variant C/A snv 0.80 3
rs10858583
LOC107984478
1.000 0.040 12 87334666 intergenic variant C/T snv 0.79 3
rs4523096
SYNE1
1.000 0.040 6 152472277 intron variant C/A snv 0.76 0.79 1