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
rs3025058
MMP3
0.658 0.600 11 102845217 upstream gene variant -/C;G ins 2.8E-04 26
rs2679757
AZIN1
0.925 0.080 8 102858590 intron variant A/G snv 0.37 2
rs26311
GHRLOS ; GHRL
1.000 0.080 3 10291242 5 prime UTR variant C/G snv 0.16 1
rs2629751
GLT8D2
0.925 0.120 12 104028030 intron variant A/G snv 0.36 2
rs548234
ATG5
0.763 0.360 6 106120159 intron variant C/T snv 0.76 11
rs61330082
NAMPT
0.732 0.320 7 106286419 upstream gene variant G/A snv 0.22 13
rs11977021 0.827 0.240 7 106288069 upstream gene variant C/T snv 0.22 5
rs510432
ATG5
0.752 0.280 6 106326155 upstream gene variant T/C snv 0.57 11
rs9514828
TNFSF13B
0.752 0.440 13 108269025 intron variant C/T snv 0.35 12
rs1469557
LOC101929248
0.925 0.120 8 10849291 downstream gene variant C/T snv 0.18 2
rs4444903
EGF
0.630 0.360 4 109912954 5 prime UTR variant A/G snv 0.51 35
rs671
ALDH2
0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs4374383
MERTK
0.776 0.200 2 112013193 intron variant A/G snv 0.58 10
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs7080536
HABP2 ; NRAP
0.683 0.360 10 113588287 missense variant G/A snv 2.2E-02 2.4E-02 27
rs236918
PCSK7
0.776 0.160 11 117220893 non coding transcript exon variant G/A;C snv 10
rs75961395
CFTR
0.763 0.280 7 117509123 missense variant G/A;T snv 4.0E-05 10
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
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs2229113
IL10RA
0.763 0.360 11 117998955 missense variant A/G snv 0.74 0.74 10
rs2645424
FDFT1
0.827 0.120 8 11826954 intron variant A/C;G snv 0.56 5
rs430397
HSPA5
0.763 0.240 9 125238840 intron variant C/T snv 9.1E-02 0.11 9
rs121918664
TERT
0.851 0.120 5 1254395 missense variant C/T snv 5.2E-05 9.1E-05 4