Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs771086543
FBXL15 ; CUEDC2
10 102422814 missense variant G/A snv 1.3E-04 1.0E-04 1
rs771799019
GRAP2
22 39969528 missense variant G/T snv 8.0E-06 7.0E-06 1
rs772903705
PSD
10 102411788 missense variant C/T snv 1
rs774390402
BCAR1
16 75235116 missense variant A/C snv 1.2E-05 1
rs777009146
CTNND1 ; TMX2-CTNND1
11 57805955 missense variant G/A snv 2.0E-05 2.8E-05 1
rs387906698
PRSS1
0.827 0.040 7 142751919 missense variant C/A;T snv 4.0E-06; 7.2E-05 8
rs1373481065
GADD45A
0.827 0.040 1 67687668 missense variant A/G snv 4.0E-06 6
rs1341667
STOX1
0.925 0.040 10 68882104 missense variant T/C snv 0.62 0.57 4
rs3917412
C1orf112 ; SELE
1.000 0.040 1 169731361 intron variant T/A;C;G snv 4
rs7240004 1.000 0.040 18 48868651 intergenic variant A/G snv 0.43 4
rs1194624468
PTK2
1.000 0.040 8 140700895 missense variant A/T snv 1.6E-05 2
rs1431090090
ZEB1
1.000 0.040 10 31520347 missense variant C/A snv 4.0E-06 2
rs1213469537
CAV1
0.882 0.080 7 116559145 missense variant C/T snv 4.0E-06 1.4E-05 9
rs1418810723
FN1
0.851 0.080 2 215409981 missense variant A/T snv 8.0E-06 9
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 6
rs3130
PROM1 ; FGFBP2
0.882 0.080 4 15968315 3 prime UTR variant T/A;C snv 6
rs78768932
PXN
0.882 0.080 12 120222977 missense variant C/G;T snv 5.4E-03 5.4E-03 6
rs1114167628
PTEN
0.925 0.080 10 87961033 stop gained -/ATATCTAG delins 5
rs1329032366
PDLIM5
0.882 0.080 4 94654530 missense variant A/G snv 4.0E-06 5
rs201701502
DDR2
0.851 0.080 1 162775837 missense variant C/G;T snv 1.5E-04 2.1E-05 5
rs374733251
MET
0.882 0.080 7 116740993 missense variant A/G snv 6.0E-05 7.7E-05 5
rs377444977
EGFR
0.882 0.080 7 55143443 missense variant G/A snv 5.2E-05 2.1E-05 5
rs61552325
ERBB2
0.882 0.080 17 39727784 missense variant C/G snv 5
rs1056123575
ADAMTS1
0.925 0.080 21 26844557 missense variant G/A snv 4.2E-06 7.0E-06 4
rs1172398253
CCN1
0.925 0.080 1 85582045 missense variant C/T snv 4.0E-06 4