Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1040177874
IDH1
0.925 0.040 2 208239914 missense variant G/A snv 4.0E-06 2
rs751857027
QTRT1
0.925 0.120 19 10707507 missense variant C/G;T snv 1.2E-05; 4.0E-06 2
rs12594
RYR2
0.925 0.040 1 237833787 3 prime UTR variant A/G snv 0.28 2
rs16835904
RYR2
0.925 0.040 1 237833954 3 prime UTR variant C/T snv 0.17 2
rs4261436
AKAP6
0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43 3
rs58064122
GFAP
0.882 0.160 17 44913334 missense variant G/A;C snv 3
rs7115578
MAML2
0.882 0.040 11 96266936 intron variant G/A snv 0.37 3
rs2431689
MIR3142HG
0.882 0.040 5 160472115 intron variant G/A snv 0.17 3
rs3745601
P2RY11 ; PPAN-P2RY11
0.882 0.120 19 10113872 missense variant G/A snv 0.16 0.13 3
rs6089953
RTEL1-TNFRSF6B ; RTEL1
0.882 0.080 20 63659655 intron variant A/G snv 0.82 3
rs867657798
TCF4
0.925 0.040 18 55631366 missense variant G/A;C snv 1.4E-05 3
rs868162712
TCF4
0.925 0.040 18 55279598 missense variant G/A snv 3
rs766727892
TCF7L2
0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06 3
rs1476157710
WNT10B
0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs2271338
ADGRL3
0.827 0.080 4 61996533 intron variant G/A snv 0.26 5
rs17522122
AKAP6
0.925 0.040 14 32833676 3 prime UTR variant G/T snv 0.41 5
rs1057519898
FGFR1
0.851 0.120 8 38417333 missense variant T/C snv 5
rs1057519899
FGFR1
0.851 0.120 8 38417879 missense variant T/C snv 5
rs866419664
TP53
0.882 0.040 17 7673821 frameshift variant -/TCCCA delins 5
rs71305152
ZFPM2
0.882 0.040 8 105437494 intron variant -/TTTTCT delins 0.43 5
rs1057519897
FGFR1
0.807 0.240 8 38414788 missense variant C/G;T snv 4.0E-06 6
rs2378456
LPP
0.807 0.200 3 188885218 3 prime UTR variant C/G;T snv 6
rs770374782
TP53
0.851 0.160 17 7673752 missense variant G/A;C snv 1.2E-05 4.2E-05 6
rs9288516
XRCC5
0.827 0.120 2 216188541 intron variant T/A snv 5.0E-02 6
rs5050
AGT
0.827 0.200 1 230714140 intron variant T/C;G snv 7