Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11638352
FRMD5
0.925 0.040 15 44000939 intron variant C/A;G snv 2
rs138741635
FHIT
0.925 0.040 3 60942161 intron variant T/A;G snv 2
rs16985615
LOC107985383
1.000 0.040 20 23661790 intron variant T/A;C snv 2
rs190543502
TP53BP1
0.925 0.040 15 43464986 intron variant T/A;C snv 2
rs201394051 0.925 0.040 5 117697919 intergenic variant TA/-;TATA;TATATA delins 2
rs2733201
FRMD5
0.925 0.040 15 44116203 intron variant T/A;C snv 2
rs559110055
ABCA1
0.925 0.160 9 104840491 missense variant A/G snv 4.0E-06 2
rs697829
KCNE5
0.925 0.160 X 109623948 3 prime UTR variant G/A snv 2
rs147642358
ARPC1A
1.000 0.040 7 99335136 intron variant G/A;T snv 1
rs747112750
LGR6
1.000 0.040 1 202307363 synonymous variant C/T snv 4.0E-06 1
rs1202989817
SOD1 ; LOC102724449
0.716 0.360 21 31659813 missense variant T/C;G snv 8.0E-06 7.0E-06 18
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1235324522
F2R
1.000 0.040 5 76732662 missense variant C/T snv 4.0E-06 1.4E-05 1
rs149232047 0.925 0.040 6 126276990 intergenic variant A/G snv 1.5E-04 2
rs188845491
CYP3A51P ; CYP3A7-CYP3A51P ; CYP3A7 ; ZSCAN25
1.000 0.040 7 99689016 intron variant C/T snv 2.5E-04 1
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs76863441
PLA2G7
0.672 0.440 6 46709361 missense variant C/A snv 4.5E-03 1.3E-03 25
rs192427471 0.925 0.040 4 124644124 intergenic variant C/T snv 2.4E-03 2
rs148121703
GABRB1
0.925 0.040 4 47371654 intron variant TGT/- delins 2.6E-03 2
rs189889864 0.925 0.040 9 104634643 downstream gene variant G/A snv 2.8E-03 2
rs61361928
UGT2B7
1.000 0.040 4 69096657 missense variant T/C snv 2.6E-03 2.8E-03 1
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs151269874
TMEM231
0.925 0.040 16 75549741 intron variant C/T snv 6.2E-03 2
rs144610116
FAM114A1
0.925 0.040 4 38941227 intron variant T/C snv 8.6E-03 2
rs117714106 0.882 0.080 14 84338144 intergenic variant C/T snv 9.1E-03 3