Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9866361
PIK3CA
0.882 0.040 3 179190061 intron variant G/A snv 0.24 3
rs454006
PRKCG
0.882 0.040 19 53886867 intron variant T/C snv 0.36 3
rs2236947
RASSF1
0.882 0.040 3 50334001 intron variant C/A snv 0.39 3
rs770771727
UTRN
0.882 0.040 6 144751941 missense variant A/C;G snv 4.5E-05; 2.5E-05 3
rs1295925
VMP1
0.882 0.040 17 59832902 intron variant T/C snv 0.60 3
rs1215600806
ALPL
0.851 0.120 1 21564100 missense variant T/C snv 1.2E-05 4
rs1416572796
ALPL
0.851 0.120 1 21568170 missense variant G/T snv 4.0E-06 4
rs143358506
ALPL
0.851 0.120 1 21560674 missense variant T/C snv 8.0E-06 7.0E-06 4
rs11866002
CNOT1
0.851 0.120 16 58553833 synonymous variant C/T snv 0.35 0.39 4
rs10019009
DMP1 ; LOC105377323
0.851 0.080 4 87661983 missense variant A/G;T snv 4.0E-06; 0.29 4
rs4150506
ERCC3
0.851 0.120 2 127262970 intron variant G/A snv 0.18 4
rs1906953
GRM4
0.882 0.040 6 34068669 intron variant C/T snv 0.25 4
rs4730222
HBP1
0.851 0.040 7 107169848 5 prime UTR variant G/A;C;T snv 4
rs16948627
ITGA3
0.882 0.040 17 50063432 intron variant C/A;T snv 4
rs2230392
ITGA3
0.882 0.040 17 50078061 missense variant G/A snv 0.14 9.0E-02 4
rs2285524
ITGA3
0.882 0.040 17 50073989 synonymous variant T/C snv 0.21 0.24 4
rs59267781
LMNA
0.851 0.120 1 156138657 missense variant C/G snv 4
rs1690916
MDM2
0.882 0.040 12 68841626 3 prime UTR variant G/A snv 0.35 4
rs7034162
NFIB
0.882 0.040 9 14190288 intron variant A/T snv 0.81 4
rs121913282
PIK3CA
0.882 0.040 3 179221072 missense variant A/C snv 4
rs7646409
PIK3CA
0.882 0.040 3 179182405 intron variant T/C snv 0.26 4
rs1253660442
SLC19A1
0.851 0.160 21 45531871 missense variant G/A;C snv 4
rs4789223
SMIM6 ; RECQL5
0.851 0.120 17 75645819 intron variant G/A snv 0.46 4
rs12602273
TP53
0.851 0.080 17 7679695 intron variant C/G snv 0.15 4
rs876660254
TP53
0.882 0.040 17 7674963 missense variant G/T snv 4