Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894104
CDKN2A
0.790 0.160 9 21971019 missense variant G/A;T snv 7
rs1049296
TF
0.882 0.120 3 133775510 missense variant C/T snv 0.16 0.14 4
rs1049793
LOC105375567 ; AOC1
0.882 0.080 7 150860577 missense variant C/G;T snv 0.37 0.37 4
rs10506095 1.000 0.040 12 32647193 downstream gene variant C/T snv 4.4E-02 1
rs1051169
S100B
0.851 0.200 21 46602317 synonymous variant C/A;G;T snv 0.65 5
rs1051308
CDIP1 ; HMOX2
0.882 0.080 16 4510300 3 prime UTR variant G/A snv 0.54 3
rs1051312
SNAP25 ; SNAP25-AS1
0.827 0.120 20 10306440 3 prime UTR variant T/C snv 0.20 5
rs10513789
MCCC1
1.000 0.040 3 183042285 intron variant T/G snv 0.22 1
rs10516839
LOC105377329
1.000 0.040 4 89587189 intron variant T/G snv 0.17 1
rs10516845
SNCA
1.000 0.040 4 89763127 intron variant A/G;T snv 1
rs1051689897
MBD5
1.000 0.040 2 148489766 synonymous variant T/C snv 8.0E-06 1
rs10518765
UNC13C
1.000 0.040 15 54388434 intron variant A/C snv 0.16 3
rs10519131
LOC107984782
1.000 0.040 15 61708933 intron variant A/C;T snv 1
rs1051931
PLA2G7
0.708 0.400 6 46705206 missense variant A/G snv 0.81 0.79 19
rs1052133
OGG1 ; CAMK1
0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1052352
FUS
0.925 0.120 16 31183958 synonymous variant C/T snv 0.53 0.45 2
rs1052551
MAPT
1.000 0.040 17 45991558 synonymous variant G/A;T snv 0.14; 8.0E-05 1
rs1052553
MAPT
0.827 0.200 17 45996523 synonymous variant A/G snv 0.14 0.15 8
rs1052587
MAPT
0.925 0.120 17 46025238 3 prime UTR variant T/C snv 0.14 3
rs1057519492
NLRP1
0.925 0.040 17 5583798 missense variant C/T snv 2
rs1058808
ERBB2
0.658 0.360 17 39727784 missense variant C/G snv 0.61 0.52 27
rs1058885
CSF1
0.925 0.080 1 109923844 missense variant T/C snv 0.38 0.39 2
rs1060499619
SYNJ1
0.851 0.040 21 32681590 missense variant C/G snv 4
rs1060501198
TP53
0.925 0.040 17 7674900 missense variant T/C;G snv 3
rs1060619
LOC112268089 ; GAPDH
1.000 0.040 12 6535615 intron variant T/C snv 0.31 1