Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3110697
IGFBP3
0.827 0.160 7 45915430 intron variant A/G snv 0.58 7
rs7372209
CTDSPL ; MIR26A1
0.807 0.160 3 37969217 intron variant T/C snv 0.77 7
rs2131877
XXYLT1
0.827 0.080 3 195137645 intron variant G/A snv 0.20 6
rs2245214
ATG5
0.827 0.240 6 106214866 intron variant C/G snv 0.42 6
rs2835267
SETD4 ; LOC100133286
0.827 0.080 21 36074727 intron variant T/C snv 0.63 6
rs5744256
IL18
0.827 0.120 11 112152125 intron variant A/G snv 0.16 6
rs7867494
RORB
0.882 0.120 9 74529284 intron variant A/G snv 0.27 6
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1470579
IGF2BP2
0.925 0.160 3 185811292 intron variant A/C snv 0.46 5
rs228729
PER3
0.827 0.120 1 7785635 intron variant T/C snv 0.69 0.69 5
rs28381975
PDCD6IP ; LOC105377023
0.827 0.200 3 33798239 intron variant -/TTACGTACCTGTGCA;TTCCGTACCTGTGCA;TTTCGTACCTGTGCA delins 5
rs3114020
ABCG2
0.882 0.200 4 88162514 intron variant T/C snv 0.40 5
rs3787728
LOC100133286 ; CBR1 ; SETD4
0.851 0.080 21 36071595 intron variant T/C snv 0.74 5
rs4488809
TP63
0.827 0.080 3 189638472 intron variant T/C snv 0.45 5
rs50872
ERCC2
0.827 0.120 19 45359191 intron variant A/G;T snv 5
rs8100239
BCL3
0.882 0.200 19 44749847 intron variant T/A snv 0.38 5
rs1143770
MIRLET7A2 ; MIR100HG
0.882 0.200 11 122146890 intron variant C/T snv 0.53 4
rs11778573
CCN4
0.851 0.080 8 133216687 intron variant T/G snv 0.59 4
rs1878022
CMKLR1
0.851 0.080 12 108305255 intron variant C/T snv 0.70 4
rs2977536
CCN4
0.851 0.080 8 133207034 intron variant G/C snv 0.36 4
rs3769821
CASP8
0.851 0.200 2 201258707 intron variant C/T snv 0.57 4
rs3782130
CYP27B1 ; METTL1
0.925 0.120 12 57768115 intron variant G/A;C snv 0.27 4
rs3805213
NOCT ; ELF2
0.851 0.080 4 139044570 intron variant C/T snv 0.23 4
rs3816769
STAT3
0.851 0.240 17 42346255 intron variant T/A;C snv 4
rs3835
XRCC5
0.882 0.120 2 216201914 intron variant G/A snv 0.21 4