Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs995922697
GPX1
0.724 0.560 3 49357413 missense variant A/G snv 4.1E-06 15
rs9395890
MLIP ; LOC101927189
0.925 0.080 6 53956196 intron variant G/A;T snv 2
rs9379084
RREB1
0.882 0.160 6 7231610 missense variant G/A snv 0.11 8.9E-02 6
rs9374
RAC1
0.925 0.080 7 6402740 3 prime UTR variant G/A snv 0.18 2
rs9369717
CD2AP
0.925 0.080 6 47586732 intron variant T/G snv 0.22 2
rs9349417
CD2AP
0.925 0.080 6 47612921 intron variant A/G snv 0.27 2
rs9298190
MSC-AS1
0.925 0.080 8 71932099 intron variant T/C snv 0.36 2
rs926632
EDN3
0.882 0.160 20 59309707 intron variant C/T snv 0.61 3
rs904520404
DCDC2
0.925 0.080 6 24302010 stop gained G/A;C snv 4.0E-06; 4.0E-06 2
rs890336
CNDP2
0.882 0.160 18 74520377 3 prime UTR variant C/G;T snv 3
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs836488
RAC1
0.925 0.080 7 6380162 intron variant C/T snv 0.13 2
rs8014363 0.882 0.160 14 53964857 downstream gene variant C/T snv 0.61 3
rs7975232
VDR
0.576 0.760 12 47845054 intron variant C/A snv 0.51 0.55 56
rs7918972
CUBN
0.925 0.080 10 16828293 intron variant T/G snv 0.15 2
rs7903146
TCF7L2
0.554 0.680 10 112998590 intron variant C/G;T snv 93
rs7830
NOS3 ; ATG9B
0.763 0.320 7 151012483 3 prime UTR variant G/T snv 0.38 0.32 11
rs777476179
ALMS1
0.851 0.280 2 73448259 frameshift variant A/- del 1.4E-05 5
rs77113398 0.925 0.080 13 106451558 intergenic variant G/A snv 6.0E-03 2
rs7708392
TNIP1
0.732 0.400 5 151077924 intron variant G/C snv 0.44 13
rs767830104
CXCR4
0.752 0.280 2 136115399 missense variant C/G;T snv 4.0E-06; 8.0E-06 13
rs7652589 0.732 0.400 3 122170241 downstream gene variant A/G snv 0.60 13
rs760452842
KLK4
0.925 0.080 19 50906983 missense variant T/G snv 4.0E-06 2
rs7588550
ERBB4
0.851 0.160 2 212304043 intron variant G/A snv 0.96 4
rs7583877
AFF3
0.925 0.080 2 99844192 intron variant C/T snv 0.61 2