Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17026425
IQCM
0.882 0.080 4 149751362 intron variant G/A snv 4.9E-02 4
rs2470151
MIR7973-2 ; CYP19A1
0.925 0.080 15 51314872 intron variant C/T snv 0.29 4
rs2737
CDK5RAP3
0.851 0.080 17 47981705 missense variant T/C snv 0.25 0.19 4
rs4998557
SOD1
0.851 0.080 21 31662579 intron variant G/A snv 0.22 4
rs664589
TALAM1 ; MALAT1
0.925 0.080 11 65501878 non coding transcript exon variant C/G snv 6.0E-02 3.8E-02 4
rs914956206
VEGFA
0.882 0.080 6 43770762 missense variant G/A;T snv 4
rs10318
GREM1
0.882 0.080 15 32733778 3 prime UTR variant C/T snv 0.16 3
rs1051424
RPS6KB1
0.925 0.080 17 59946963 3 prime UTR variant A/G snv 0.15 3
rs1194338 0.925 0.080 11 65493967 upstream gene variant C/A;T snv 3
rs1230416942
TTI2 ; MAK16
0.925 0.080 8 33498547 missense variant G/C snv 7.0E-06 3
rs150742660
NCAPH2 ; SCO2
0.925 0.080 22 50523735 missense variant A/G snv 8.0E-06 3
rs1625649
MGMT
0.882 0.080 10 129466667 upstream gene variant A/C snv 0.61 3
rs2070804
HSPB1
0.925 0.080 7 76304395 downstream gene variant T/G snv 0.13 3
rs2306536
CHFR
0.925 0.080 12 132847076 missense variant C/T snv 0.18 0.21 3
rs2632159
LOC105375751 ; PCAT1
0.882 0.080 8 127021159 intron variant G/A;T snv 3
rs34296044
EXO1
0.925 0.080 1 241885371 frameshift variant C/- delins 3
rs353292
MIR143 ; CARMN
0.882 0.080 5 149428245 non coding transcript exon variant G/A snv 0.35 3
rs370662884
CTNNB1
0.925 0.080 3 41225816 synonymous variant G/A snv 3.2E-05 4.9E-05 3
rs372032595
DLD
0.925 0.080 7 107904960 missense variant T/G snv 4.0E-06 3
rs756045117
MLH1
0.925 0.080 3 37012090 missense variant C/G;T snv 1.6E-05 3
rs1052748
PLD2
0.925 0.080 17 4817174 missense variant C/T snv 0.39 0.36 2
rs1063169
FOS
0.925 0.080 14 75280415 5 prime UTR variant G/T snv 0.12 2
rs1065411
GSTM2 ; GSTM1
0.925 0.080 1 109690516 missense variant G/A;C;T snv 0.36; 6.9E-06 2
rs10845671
GPRC5D-AS1
0.925 0.080 12 12926708 upstream gene variant C/A;T snv 2
rs10883782
WBP1L
0.925 0.080 10 102824175 intron variant A/G snv 0.14 2