Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs8193037
IL17A
0.752 0.320 6 52186311 upstream gene variant G/A;T snv 12
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs1800779
NOS3
0.763 0.320 7 150992855 intron variant G/A;C snv 9
rs10401969
SUGP1
0.776 0.240 19 19296909 intron variant T/C snv 0.10 25
rs5068
NPPA ; NPPA-AS1 ; CLCN6
0.776 0.160 1 11845917 3 prime UTR variant A/G;T snv 13
rs4819554
IL17RA
0.776 0.320 22 17084145 upstream gene variant G/A snv 0.84 10
rs4506565
TCF7L2
0.790 0.280 10 112996282 intron variant A/G;T snv 22
rs3745297
HRC
0.790 0.120 19 49154952 missense variant A/C snv 0.41 0.38 10
rs7626962
SCN5A
0.790 0.080 3 38579416 missense variant G/A;T snv 1.6E-05; 5.9E-03 10
rs3766871
RYR2
0.790 0.240 1 237614784 missense variant G/A;T snv 4.0E-02 9
rs121918090
TTR
0.790 0.240 18 31593026 missense variant G/C snv 8
rs140226130
CCDC178
0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs4803750
BCL3
0.807 0.240 19 44744370 upstream gene variant A/G snv 7.7E-02 22
rs562338 0.807 0.160 2 21065449 intergenic variant A/G snv 0.69 21
rs2074755
BAZ1B
0.807 0.240 7 73462836 non coding transcript exon variant T/C snv 9.2E-02 20
rs10423928
GIPR
0.807 0.200 19 45679046 intron variant T/A snv 0.19 12
rs111033560
PLN ; CEP85L
0.807 0.040 6 118559037 stop gained T/G snv 1.6E-05 9
rs911119
CST3
0.807 0.120 20 23632100 non coding transcript exon variant C/G;T snv 9
rs9943582
APLNR
0.807 0.120 11 57237593 upstream gene variant T/C snv 0.63 8
rs2230345
GRK5
0.807 0.160 10 119326585 missense variant A/T snv 3.8E-02 9.0E-02 6
rs371401403
MYBPC3
0.807 0.080 11 47335996 missense variant G/A;T snv 6.8E-05; 7.9E-05 6
rs587782951
JPH2
0.807 0.080 20 44160305 missense variant G/T snv 6
rs247617 0.827 0.160 16 56956804 regulatory region variant C/A snv 0.29 20
rs1728918 0.827 0.160 2 27412596 upstream gene variant A/G;T snv 19
rs765547 0.827 0.160 8 20008763 intergenic variant G/A;C;T snv 18