Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12778366
SIRT1
0.724 0.480 10 67883321 upstream gene variant T/C;G snv 13
rs1800955
DRD4
0.827 0.160 11 636784 upstream gene variant T/C;G snv 8
rs2287161
MTERF2
0.827 0.080 12 106987362 upstream gene variant C/G;T snv 7
rs4880213 0.827 0.160 9 137136549 upstream gene variant C/G;T snv 6
rs2990245
GBAP1
0.827 0.240 1 155227671 upstream gene variant C/G;T snv 5
rs4704559 0.925 0.080 5 79517086 upstream gene variant A/G snv 0.15 4
rs3758549
GBF1
0.882 0.040 10 102244438 upstream gene variant G/A snv 0.14 3
rs823114
NUCKS1
1.000 0.040 1 205750404 upstream gene variant G/A snv 0.45 3
rs823118 0.925 0.080 1 205754444 upstream gene variant C/A;T snv 3
rs1362858
LOC105372063
0.925 0.040 18 35406636 upstream gene variant C/A snv 0.71 2
rs1876487
SPR
1.000 0.040 2 72887223 upstream gene variant A/C snv 0.54 2
rs13362909
LINGO2
1.000 0.040 9 27945981 upstream gene variant C/A;T snv 1
rs1438852 1.000 0.040 2 118838515 upstream gene variant C/T snv 0.52 1
rs1504212 1.000 0.040 5 53824125 upstream gene variant C/A snv 0.51 1
rs2421095
SPR
1.000 0.040 2 72886395 upstream gene variant G/A snv 0.86 1
rs2987763
PGLYRP3
1.000 0.040 1 153313558 upstream gene variant T/A snv 0.42 1
rs3014864
PGLYRP4
1.000 0.040 1 153349108 upstream gene variant G/C;T snv 1
rs30196
LOC105379041 ; SV2C
1.000 0.040 5 76081726 upstream gene variant G/T snv 0.57 1
rs34372695
RAB25
1.000 0.040 1 156060246 upstream gene variant C/G;T snv 1.5E-02 1
rs6532197 1.000 0.040 4 89876150 upstream gene variant A/G snv 0.16 1
rs9268515 1.000 0.040 6 32411518 upstream gene variant G/C snv 0.16 1
rs9858038 1.000 0.040 3 183012503 upstream gene variant G/A snv 0.22 1
rs776070150
THBS3 ; MTX1
1.000 0.040 1 155208977 inframe deletion CGTGACTCTCCGAGGCGC/- delins 1
rs16940665
MAPT-AS1 ; LINC02210-CRHR1 ; CRHR1
1.000 0.040 17 45830530 stop lost T/C snv 0.15 0.14 2
rs2228570
VDR
0.521 0.760 12 47879112 start lost A/C;G;T snv 0.63 99