Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17115149
CYP17A1
0.882 0.160 10 102837961 upstream gene variant G/A;T snv 4
rs2296147
BIVM-ERCC5 ; ERCC5
0.695 0.280 13 102846025 5 prime UTR variant T/C snv 0.38 21
rs5498
ICAM4 ; ICAM1
0.531 0.760 19 10285007 missense variant A/G snv 0.44 0.37 99
rs1047768
ERCC5 ; BIVM-ERCC5
0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs17655
BIVM-ERCC5 ; ERCC5
0.597 0.560 13 102875652 missense variant G/C snv 0.28 0.30 52
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1799796
XRCC3 ; KLC1
0.790 0.240 14 103699590 intron variant T/A;C snv 0.31 7
rs141752671 0.708 0.280 11 103745837 intron variant A/G snv 5.4E-03 17
rs148883465 0.708 0.280 11 103813371 intron variant A/G snv 7.2E-03 17
rs200182588
SMC2-AS1 ; SMC2
0.827 0.160 9 104094409 5 prime UTR variant -/GC ins 7.0E-06 6
rs156113 0.925 0.080 6 104369868 intergenic variant A/T snv 0.96 2
rs2494732
AKT1
0.763 0.240 14 104772855 intron variant T/C snv 0.50 0.47 11
rs3730358
AKT1
0.724 0.360 14 104780070 intron variant G/A;C snv 0.16; 4.0E-03 14
rs121434592
AKT1
0.595 0.640 14 104780214 missense variant C/T snv 4.0E-06 54
rs636291
PEX14
0.925 0.080 1 10496040 intron variant G/A snv 0.55 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs1221877686
TET2-AS1 ; TET2
0.925 0.080 4 105234193 missense variant G/A snv 2
rs9287719
NOL10
1.000 0.080 2 10570604 downstream gene variant C/T snv 0.60 1
rs12315175 0.925 0.080 12 107105494 intron variant T/C snv 0.18 2
rs1283104
DUBR
1.000 0.080 3 107243674 intron variant C/G snv 0.43 1
rs817826 0.925 0.080 9 107394019 intergenic variant C/T snv 0.81 2
rs4988483
SSTR5-AS1 ; SSTR5
0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11
rs2237706
LAMB1
1.000 0.080 7 107992726 intron variant C/T snv 7.5E-02 1
rs197056
SSTR5
0.925 0.080 16 1081695 upstream gene variant A/C;G snv 2
rs197057 0.925 0.080 16 1082015 upstream gene variant C/G snv 0.53 2