Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4919510
SEMA4G ; MIR608 ; MRPL43
0.641 0.520 10 100975021 mature miRNA variant C/G snv 0.27 0.27 32
rs12769316
NFKB2
0.925 0.160 10 102392994 upstream gene variant G/A snv 0.13 3
rs28362491
LOC105377621 ; NFKB1
0.592 0.720 4 102500998 non coding transcript exon variant ATTG/- delins 56
rs1799750
WTAPP1 ; MMP1
0.592 0.760 11 102799765 intron variant C/- delins 0.50 48
rs4771436
BIVM-ERCC5 ; ERCC5
1.000 0.120 13 102849670 intron variant T/G snv 0.22 1
rs4699052 0.925 0.200 4 103216633 intergenic variant C/T snv 0.44 3
rs861539
KLC1 ; XRCC3
0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs9295535
MIR5689HG ; MIR5689
0.851 0.160 6 10439735 mature miRNA variant T/C snv 0.30 0.20 4
rs1130233
AKT1
0.742 0.480 14 104773557 synonymous variant C/T snv 0.30 0.23 13
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 28
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39
rs17483466
MIR4435-2HG ; ACOXL
0.827 0.280 2 111039881 intron variant A/G snv 0.15 5
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs4938723
MIR34C ; BTG4 ; MIR34B ; LOC728196
0.574 0.680 11 111511840 intron variant T/C snv 0.32 60
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs3740194
CELF2
1.000 0.120 10 11255346 intron variant T/C snv 0.47 1
rs3783553
IL1A
0.667 0.480 2 112774138 3 prime UTR variant -/TGAA delins 26
rs7804372
CAV1
0.716 0.320 7 116554174 intron variant T/A snv 0.27 19
rs2089222
MAP1LC3B2
0.925 0.200 12 116564853 intron variant G/A snv 0.12 2
rs16892766 0.716 0.240 8 116618444 intergenic variant A/C snv 9.3E-02 18
rs4986790
TLR4
0.438 0.800 9 117713024 missense variant A/G;T snv 6.1E-02; 4.0E-06 223
rs4986791
TLR4
0.456 0.840 9 117713324 missense variant C/T snv 5.7E-02 4.9E-02 182
rs498872
PHLDB1
0.776 0.240 11 118606652 5 prime UTR variant A/G;T snv 10
rs3755557
GSK3B ; LOC107986119
0.807 0.280 3 120096110 non coding transcript exon variant T/A snv 0.14 6
rs11249433
EMBP1
0.827 0.160 1 121538815 intron variant A/C;G snv 9