Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs900147 11 13272293 upstream gene variant G/A snv 0.62 1
rs76732092
GTF2H1
11 18358030 missense variant C/A snv 1
rs6600879
UGT2B7
4 69094669 intron variant C/G snv 0.58 1
rs6600880
UGT2B7
4 69094762 intron variant T/A snv 0.58 1
rs281865051
LRRK2
1.000 0.040 12 40319998 missense variant T/C snv 2
rs12593813
MAP2K5
1.000 0.080 15 67744514 intron variant A/G snv 0.53 2
rs35986369
RAB5A
1.000 0.040 3 19950975 frameshift variant -/GG delins 2
rs4292394
UGT2B7
4 69107231 synonymous variant C/G snv 0.56 0.59 2
rs6600893
UGT2B7
4 69113183 downstream gene variant T/C snv 0.59 2
rs1564282
GAK
1.000 0.040 4 858525 intron variant C/T snv 8.1E-02 3
rs34016896
LOC105374187
0.925 0.080 3 161275076 regulatory region variant C/T snv 0.28 3
rs564856283
MYBPC1
12 101642495 missense variant G/A;C snv 3.2E-05 3
rs80356727
TARDBP
0.925 0.080 1 11022400 missense variant C/A snv 3
rs3810651
GABRQ ; LOC105373370
0.925 0.080 X 152652814 missense variant A/C;T snv 4
rs1057518839
MPZ
1.000 1 161305924 missense variant A/C snv 4
rs587777721
SCN8A
0.925 0.160 12 51806336 missense variant G/A snv 4
rs104894158
EGR2
0.851 0.080 10 62813835 missense variant A/T snv 5
rs786205232
KCNA2
0.925 0.040 1 110603893 missense variant C/T snv 4.0E-06 5
rs869312713
ANKRD11
0.882 0.320 16 89280070 stop gained C/A snv 6
rs200455852
ASAH1
0.851 0.200 8 18064458 missense variant T/C;G snv 5.8E-05 6
rs3794087
SLC1A2
0.851 0.120 11 35308068 intron variant G/T snv 0.20 6
rs139194636
WARS2
0.882 0.240 1 119033203 missense variant T/C snv 6.4E-05 2.3E-04 6
rs757600616
WARS2
0.882 0.240 1 119033279 stop gained G/A snv 1.2E-05 6
rs146170087
C19orf12
0.925 0.040 19 29702747 missense variant T/C snv 2.3E-03 1.1E-03 7
rs515726205
C19orf12
0.882 0.040 19 29702966 missense variant C/T snv 2.4E-05 1.4E-05 7