Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9387479
DCBLD1
1.000 0.040 6 117471449 intron variant T/C;G snv 1
rs397507444
MTHFR
0.405 0.880 1 11794407 missense variant T/G snv 306
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs55768116
MPZL3
0.925 0.080 11 118237616 intron variant C/A snv 0.38 2
rs1056562
MPZL2
1.000 0.040 11 118254910 3 prime UTR variant T/C snv 0.57 1
rs114928225 1.000 0.040 2 118692164 intergenic variant T/A snv 1.0E-02 1
rs1458974438
STK11
0.807 0.080 19 1206957 missense variant G/A snv 9
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 7
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 7
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 19
rs121913315
STK11
0.882 0.160 19 1220488 missense variant G/A;T snv 5
rs1057520017
STK11
1.000 0.040 19 1220630 missense variant C/T snv 1
rs754284524
SRFBP1 ; LOX
1.000 0.040 5 122074125 stop gained -/TACATGCTAGATTCATTTTAACTCAATACTGCCATTCAATTCTAGCAAC ins 4.0E-06 2
rs7977932
LRRC43 ; IL31
0.763 0.320 12 122172836 intron variant C/G;T snv 10
rs80338796
RAF1
0.667 0.480 3 12604200 missense variant G/A;C snv 4.0E-06 37
rs1026411
LOC105375751 ; PCAT1
0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1057519918
CASC11 ; MYC
0.851 0.200 8 127738390 missense variant C/T snv 5
rs750664148
CASC11 ; MYC
0.851 0.200 8 127738434 missense variant A/C;G snv 5
rs756091827
MYC ; CASC11
0.851 0.200 8 127738435 missense variant C/G;T snv 6
rs2608029
PVT1
1.000 0.040 8 128157880 intron variant C/G snv 0.37 2
rs7725218
TERT
0.708 0.280 5 1282299 intron variant G/A snv 0.38 17
rs67824503
LINC00824
1.000 0.040 8 128523018 intron variant T/C snv 0.23 1
rs7705526
TERT
0.776 0.240 5 1285859 intron variant C/A;T snv 15