Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10165970
NPAS2
0.708 0.320 2 100840527 intron variant G/A snv 0.16 18
rs17024869
NPAS2
0.708 0.320 2 100843581 intron variant T/C snv 8.3E-02 18
rs895520
NPAS2
0.689 0.320 2 100961475 intron variant G/A snv 0.35 23
rs7581886
NPAS2
0.708 0.320 2 100964784 intron variant C/T snv 0.92 18
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs2281611
MEG8 ; MIR495
0.925 0.080 14 101033612 intron variant G/A;T snv 2
rs763351020
SERPINE1
0.633 0.560 7 101132046 missense variant C/T snv 4.0E-06 35
rs1419316960
DNMT1
0.925 0.080 19 10166651 missense variant T/C snv 7.0E-06 2
rs823920 0.925 0.080 9 101900303 intergenic variant A/G snv 0.12 2
rs35060588
IRAK2
0.925 0.080 3 10213318 missense variant C/G;T snv 5.5E-02; 1.6E-05 2
rs1215486792
MOK
0.925 0.080 14 102229572 missense variant C/G snv 7.0E-06 2
rs11704
CINP ; ZNF839
0.925 0.080 14 102342318 3 prime UTR variant G/C snv 0.26 2
rs2946834
LINC02456 ; HELLPAR
0.807 0.200 12 102394036 non coding transcript exon variant A/G snv 0.63 7
rs6214
LINC02456 ; HELLPAR ; IGF1
0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs867538330
SLCO6A1
0.925 0.080 5 102458457 synonymous variant C/T snv 2
rs35767
IGF1 ; LOC105369944
0.763 0.360 12 102481791 upstream gene variant A/C;G;T snv 13
rs750521832
MMP8
0.732 0.200 11 102718452 missense variant A/G snv 4.0E-06 14
rs10883782
WBP1L
0.925 0.080 10 102824175 intron variant A/G snv 0.14 2
rs17724534
LOC107984264
0.925 0.080 10 102845764 non coding transcript exon variant C/T snv 9.1E-02 2
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
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
rs156697
GSTO2
0.672 0.560 10 104279427 missense variant A/G;T snv 0.35 25
rs2302615
ODC1-DT ; SNORA80B ; ODC1
0.807 0.120 2 10448012 intron variant C/T snv 0.31 7