Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2132572
IGFBP3
1.000 7 45921946 upstream gene variant T/C snv 0.79 3
rs9400239
FOXO3
1.000 6 108656460 5 prime UTR variant T/C snv 0.55 3
rs10136427
LOC105370572
0.925 14 75513546 intergenic variant C/T snv 0.21 2
rs1220597
SPATA13
0.925 13 24243875 intron variant C/T snv 0.51 2
rs13184587
ARSB
0.925 5 78910960 intron variant G/A;T snv 2
rs16962916 0.925 16 13806476 intergenic variant A/C;G snv 2
rs17739370 0.925 4 177374275 intergenic variant C/T snv 0.38 2
rs2048722
TPO
0.925 2 1492028 intron variant A/G snv 0.51 2
rs3136166
ERCC4
0.925 16 13938236 intron variant T/G snv 0.44 2
rs371428527
PIK3CB
0.925 3 138737869 missense variant T/C;G snv 1.2E-05 1.4E-05 2
rs7267944 0.925 20 39318791 intergenic variant T/C snv 0.25 2
rs7689099
NEIL3
0.925 4 177335759 missense variant C/A;G;T snv 4.2E-06; 0.11; 1.7E-05 2
rs1302723597
GGCT
1.000 7 30497778 missense variant A/C;G snv 8.1E-06; 8.1E-06 1
rs2480258
CYP2E1
1.000 10 133538596 intron variant T/C snv 0.63 1
rs34081947
LOC105370451 ; LINC00609
1.000 14 36090325 intron variant C/T snv 0.44 1
rs3828599
GPX3 ; LOC105378228
0.882 0.040 5 151022235 intron variant A/G snv 0.67 5
rs768827923
PIK3CD
0.851 0.080 1 9721816 missense variant T/G snv 6
rs71369530
FOXE1 ; PTCSC2
0.851 0.080 9 97854419 inframe insertion GCCGCCGCCGCCGCCGCCGCCGCC/-;GCC;GCCGCC;GCCGCCGCC;GCCGCCGCCGCC;GCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC;GCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCCGCC delins 0.68 4
rs1800860
RET
0.882 0.080 10 43111239 missense variant A/G snv 0.70 0.74 3
rs4915076
VAV3
0.882 0.080 1 107816883 intron variant T/C snv 9.1E-02 3
rs10808556
CASC8 ; POU5F1B ; PCAT1 ; CCAT2
0.925 0.080 8 127400902 non coding transcript exon variant C/T snv 0.50 2
rs11175834
LINC02454 ; LOC100507065
0.925 0.080 12 65598856 intron variant C/T snv 0.14 2
rs12990503
DIRC3
0.925 0.080 2 217429494 intron variant C/G snv 0.64 2
rs1874564
LOC107986291 ; LOC105377294
0.925 0.080 4 76936952 intergenic variant G/A snv 0.58 2
rs4649295
PCNX2
0.925 0.080 1 233280792 intron variant T/C snv 0.60 2