Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13016963
FLACC1
0.851 0.080 2 201298088 intron variant A/G snv 0.59 5
rs132985
PLA2G6
0.827 0.120 22 38167464 intron variant C/T snv 0.51 5
rs16953002
FTO
0.882 0.080 16 54080912 intron variant G/A snv 0.19 5
rs4845618
IL6R
0.851 0.160 1 154427539 intron variant G/T snv 0.53 5
rs10754833
NID1
0.851 0.040 1 236021631 intron variant T/A;C snv 4
rs10830253
TYR
0.851 0.080 11 89294875 intron variant T/G snv 0.29 4
rs1155563
GC
0.925 0.080 4 71777771 intron variant T/A;C snv 4
rs1636744
AHR
0.851 0.080 7 16944656 intron variant C/T snv 0.31 4
rs2284378
RALY
0.851 0.080 20 34000289 intron variant T/C;G snv 4
rs2995264
STN1
0.851 0.080 10 103909085 intron variant G/A snv 0.88 4
rs6750047
RMDN2
0.851 0.080 2 38049406 intron variant A/G snv 0.61 4
rs6914598
CDKAL1
0.851 0.080 6 21163688 intron variant T/C snv 0.38 4
rs75570604
FANCA
0.851 0.080 16 89780269 intron variant G/C snv 4.7E-02 4
rs869329
MTAP
0.851 0.080 9 21804694 intron variant A/G;T snv 4
rs10757257
MTAP
0.882 0.080 9 21806565 intron variant G/A snv 0.34 3
rs12418451
LOC338694 ; LOC105369366
0.882 0.080 11 69167951 intron variant G/A snv 0.22 3
rs139996880
TERT
0.882 0.120 5 1284538 intron variant G/A snv 0.12 3
rs1847134
LOC107984363 ; TYR
0.925 0.080 11 89272085 intron variant A/C snv 0.26 3
rs222016
GC
0.882 0.120 4 71769258 intron variant G/A snv 0.72 3
rs258322
CDK10
0.925 0.120 16 89689495 intron variant A/G;T snv 3
rs910873
PIGU
0.882 0.160 20 34583968 intron variant G/A;C snv 3
rs1885120
LOC107985393 ; MIR499A ; MYH7B
1.000 0.040 20 34989186 intron variant C/G snv 0.96 2
rs1990330
TEAD4
0.925 0.080 12 3038296 intron variant A/C;T snv 2
rs2074560
MX2
0.925 0.040 21 41380411 intron variant A/G snv 0.43 2
rs215605
PDE1C
1.000 0.040 7 32297353 intron variant G/T snv 0.54 2