Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs743572
CYP17A1
0.672 0.360 10 102837395 5 prime UTR variant A/G;T snv 0.40; 8.1E-06 24
rs115336889
ROPN1L
1.000 0.040 5 10454257 intron variant G/A;C snv 1
rs10786938 1.000 0.040 10 106280012 intergenic variant G/C;T snv 1
rs36067435
ELOVL6
1.000 0.040 4 110180390 intron variant -/TTAT delins 1
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs10054105
STARD4-AS1
0.925 0.080 5 111573636 intron variant T/G snv 0.17 3
rs2555019 1.000 0.040 12 114230813 intergenic variant T/C;G snv 3
rs8853
TBX3
0.882 0.120 12 114671102 3 prime UTR variant T/C snv 0.52 4
rs339331
RFX6
0.882 0.080 6 116888889 intron variant T/C snv 0.28 4
rs10983755 0.790 0.320 9 117702392 upstream gene variant G/A snv 3.2E-02 7
rs1927907
TLR4
0.790 0.320 9 117710486 intron variant C/T snv 0.18 7
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs4548546
WDR11
1.000 0.040 10 120870067 intron variant C/G;T snv 3
rs11199879 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 3
rs1047100
FGFR2
1.000 0.040 10 121538644 synonymous variant T/A;C snv 1.2E-05; 0.78 1
rs2981575
FGFR2
0.882 0.120 10 121586602 intron variant G/A snv 0.54 4
rs6078585 1.000 0.040 20 12447612 intergenic variant C/A;T snv 1
rs2853677
TERT
0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 19
rs2736098
TERT
0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs78105154
ELAC2
0.925 0.080 17 12994991 missense variant G/A snv 3.2E-04 7.0E-05 2
rs5030739
ELAC2
0.776 0.160 17 12996585 missense variant C/T snv 3.5E-02 2.9E-02 8
rs4792311
ELAC2
0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 9
rs381949
CLPTM1L
1.000 0.040 5 1322353 intron variant G/A snv 0.44 3
rs677394
C5orf66
1.000 0.040 5 135271869 intron variant G/C;T snv 2