Source: GWASCAT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2797436
RYR2
0.925 0.040 1 237700418 synonymous variant T/A;G snv 7.0E-05; 0.99 2
rs6670122
MRPL24
0.882 0.120 1 156737983 intron variant T/C;G snv 0.99 2
rs10915816
DNAH14
0.925 0.040 1 225374683 splice region variant C/T snv 0.81 0.73 2
rs730819
VPS16 ; PTPRA
0.925 0.040 20 2864484 intron variant G/A snv 0.43 0.37 2
rs7653834
PLCL2
0.925 0.040 3 17009836 synonymous variant T/C snv 0.37 0.38 2
rs217373
DDX56
0.925 0.040 7 44572855 intron variant C/A;T snv 0.36 2
rs9352613 0.925 0.040 6 78714716 intergenic variant A/G snv 0.34 0.30 2
rs11205303
MTMR11
0.882 0.120 1 149934520 missense variant T/C snv 0.33 0.29 8
rs25673
AP3D1
0.925 0.040 19 2109158 missense variant T/C;G snv 0.12; 4.8E-04 2
rs4597312
TANGO6
0.925 0.040 16 68860050 synonymous variant T/A;C;G snv 4.0E-06; 0.11; 4.0E-06 2
rs9680823
RTCB
0.925 0.040 22 32394994 intron variant C/G;T snv 8.6E-02; 4.3E-06 2
rs1816522
PLCH1
0.925 0.040 3 155482774 synonymous variant G/A;T snv 2.0E-04; 5.3E-02 2
rs6671070
CCDC18
0.925 0.040 1 93217906 intron variant G/A snv 2.4E-02 9.5E-02 2
rs11466648
TLR10
0.925 0.040 4 38775321 synonymous variant T/C snv 7.0E-03 2.9E-02 2
rs6463483
FBXL18
0.925 0.040 7 5491212 intron variant C/T snv 6.9E-03 3.2E-02 2
rs9321309
ENPP3
0.925 0.040 6 131726105 missense variant G/A snv 5.1E-03 2.2E-02 2
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 11
rs10830963
MTNR1B
0.776 0.400 11 92975544 intron variant C/G snv 0.22 7
rs11157436
TRAV30
0.851 0.040 14 22168978 synonymous variant C/T snv 0.19 7
rs6570507
ADGRG6
0.827 0.240 6 142358435 intron variant G/A snv 0.47 7
rs10052657
PDE4D
0.807 0.120 5 59111944 intron variant C/A snv 0.17 4
rs2816992
NR5A2 ; LOC107985244
0.925 0.040 1 200100088 intron variant A/G snv 0.39 4
rs545608
CRYZL2P-SEC16B ; SEC16B
0.925 0.040 1 177929986 intron variant G/C snv 0.20 4
rs10739217
LOC107987108
0.925 0.040 9 105973112 regulatory region variant T/A;C snv 3
rs11190870 0.827 0.200 10 101219450 intergenic variant T/A;C snv 3