Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs767964519
NFE2L2
0.925 0.120 2 177231869 missense variant T/C snv 4.0E-06 2
rs1034925236
NR5A2
0.925 0.120 1 200048258 missense variant G/C snv 2
rs138147246
OGG1
0.925 0.120 3 9756551 synonymous variant A/G snv 8.0E-06 1.4E-05 2
rs139632793
OGG1
0.925 0.120 3 9751114 missense variant G/C snv 5.2E-05 1.7E-04 2
rs145574072
OGG1
0.925 0.120 3 9754765 synonymous variant T/C snv 4.0E-06 2
rs149243735
OGG1
0.925 0.120 3 9751076 missense variant C/A snv 4.0E-06 2
rs5757573
PDGFB
0.925 0.120 22 39237617 intron variant C/T snv 0.57 2
rs1235228469
PIK3CB
0.925 0.120 3 138684714 missense variant C/A snv 8.0E-06 2
rs1412335442
PIK3CG
0.925 0.120 7 106868317 missense variant G/T snv 7.0E-06 2
rs1448106115
PMS2
0.925 0.120 7 5989944 missense variant T/C snv 4.0E-06 2
rs34852782
PRKAG2
0.925 0.120 7 151869086 intron variant -/A;AG ins 2
rs3751936
RPTOR
0.925 0.120 17 80964404 3 prime UTR variant G/C snv 0.20 2
rs62068300
RPTOR
0.925 0.120 17 80600927 intron variant G/A;T snv 5.7E-05 2
rs10500715
SBF2
0.925 0.120 11 9951515 intron variant T/G snv 0.39 2
rs12362504
SBF2 ; LOC101928008
0.925 0.120 11 9907995 intron variant T/C snv 0.37 2
rs2074733
SF3A1
0.925 0.120 22 30342598 non coding transcript exon variant T/C snv 0.53 2
rs2457571
SLC22A3
0.925 0.120 6 160413796 intron variant T/C snv 0.62 2
rs17458086
SLC2A13
0.925 0.120 12 40034837 intron variant T/C snv 1.1E-02 2
rs3124761
SLC2A6
0.925 0.120 9 133474633 intron variant T/C snv 0.80 2
rs1630747
SLC5A3 ; MRPS6
0.925 0.120 21 34085692 intron variant C/A snv 0.69 2
rs4149086
SLCO1B1
0.925 0.120 12 21239517 3 prime UTR variant A/G snv 4.5E-04 2
rs11085754
SMARCA4
0.925 0.120 19 11017920 intron variant A/G snv 0.41 2
rs2073389
SMARCB1
0.925 0.120 22 23791306 intron variant C/T snv 0.59 2
rs779731636
SOD2
0.925 0.120 6 159685026 missense variant C/A snv 8.6E-06 2
rs4988487
SSTR5 ; SSTR5-AS1
0.925 0.120 16 1079193 missense variant C/A;T snv 4.0E-06; 5.3E-02 2