Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12476147
ZNF804A
0.851 0.040 2 184936178 missense variant A/T snv 0.66 0.59 4
rs2302045
MTERF4 ; SNED1
0.851 0.040 2 241081801 splice region variant G/A snv 7.6E-02 1.0E-01 4
rs6740584
CREB1
0.882 0.040 2 207564627 intron variant T/C snv 0.37 4
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 3
rs78087832 0.925 0.040 2 224600060 intergenic variant C/T snv 2.4E-03 3
rs2551941
METTL21A
0.925 0.040 2 207627419 upstream gene variant A/G;T snv 2
rs53576
OXTR ; CAV3
0.641 0.320 3 8762685 intron variant A/G;T snv 42
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs9825823
FHIT
0.851 0.080 3 61096480 intron variant T/C snv 0.47 5
rs2199503
GSK3B
0.851 0.080 3 120059642 intron variant T/C snv 0.79 4
rs9862857
LOC101927995 ; LOC105377013
0.851 0.040 3 30453840 regulatory region variant A/G;T snv 4
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs139459337
ZBTB20
0.882 0.040 3 114997018 intron variant C/T snv 4.7E-02 3
rs142484554
SPSB4
0.925 0.040 3 141059454 intron variant GAG/- delins 0.11 3
rs2137947
LOC105376934
0.882 0.040 3 4989276 downstream gene variant C/T snv 0.64 3
rs334535
GSK3B
0.882 0.040 3 120073457 intron variant C/T snv 0.29 3
rs6771023
GSK3B
0.882 0.040 3 119974764 intron variant T/C snv 0.22 3
rs4685959 0.925 0.040 3 5645577 regulatory region variant C/G;T snv 2
rs76767803 0.925 0.040 3 36230378 intergenic variant C/T snv 0.16 2
rs6857715
NPY2R ; LOC107986321
0.827 0.160 4 155208030 non coding transcript exon variant C/A;T snv 5
rs12649507
CLOCK
0.851 0.080 4 55514317 intron variant G/A;T snv 4
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs11728985
C4orf33
0.925 0.040 4 129115280 3 prime UTR variant C/T snv 0.12 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3