Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2189517
RAD51B
0.882 0.080 14 68536271 intron variant A/G snv 0.49 3
rs1503185
PTPRJ
0.807 0.120 11 48125070 missense variant G/A snv 0.18 0.19 8
rs5273
PTGS2
0.827 0.080 1 186674636 missense variant A/C;G snv 4.0E-06; 7.6E-03 1.4E-02 6
rs13254738
PRNCR1 ; CASC19 ; PCAT1
0.807 0.160 8 127092098 non coding transcript exon variant C/A;T snv 8
rs1967327
PRKRA ; PJVK
0.925 0.080 2 178449632 intron variant G/A;C;T snv 2
rs8905
PRKAR1A ; FAM20A
0.925 0.080 17 68531661 3 prime UTR variant T/A;G snv 2
rs1801282
PPARG
0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 131
rs1805192
PPARG
0.510 0.840 3 12379739 missense variant C/G snv 121
rs1450081432
PMS2
0.851 0.120 7 5987230 missense variant C/T snv 4.0E-06 4
rs1060503118
PMS2
0.925 0.080 7 5987422 missense variant C/T snv 2
rs587782513
PMS2
0.925 0.080 7 5992023 missense variant T/C;G snv 4.0E-06 2
rs762100304
PMS2
0.925 0.080 7 5987005 missense variant C/A;T snv 2
rs3730089
PIK3R1
0.827 0.280 5 68292320 missense variant G/A snv 0.18 0.22 5
rs752021744
PIK3CB
0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs121913273
PIK3CA
0.605 0.440 3 179218294 missense variant G/A;C snv 44
rs1902432
PCAT1 ; LOC105375751
0.851 0.120 8 127012566 intron variant A/G snv 0.25 4
rs6983267
PCAT1 ; CCAT2 ; CASC8 ; POU5F1B
0.578 0.440 8 127401060 non coding transcript exon variant G/T snv 0.37 62
rs1136410
PARP1
0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs3219145
PARP1
0.882 0.120 1 226363128 missense variant T/C;G snv 1.2E-02; 4.0E-06 4
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs756363791
OGG1
0.882 0.080 3 9756823 missense variant G/A snv 2.0E-05 4
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7
rs374400
OBSCN
0.925 0.080 1 228347383 intron variant C/T snv 0.40 2
rs1800566
NQO1
0.576 0.680 16 69711242 missense variant G/A snv 0.25 0.21 59
rs2297518
NOS2
0.658 0.480 17 27769571 missense variant G/A snv 0.18 0.17 30