Source: BEFREE ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9557635
NALCN
1.000 0.040 13 101398739 intron variant A/G snv 0.70 1
rs193100333
YAP1
1.000 0.040 11 102209523 missense variant C/T snv 3.0E-04 1.1E-04 1
rs11591710 0.882 0.160 10 103927874 intergenic variant A/C snv 0.16 2
rs7679673 0.677 0.440 4 105140377 intron variant C/A snv 0.50 5
rs189037
ATM ; NPAT
0.689 0.400 11 108223106 5 prime UTR variant G/A snv 0.49 22
rs611646
ATM
0.882 0.120 11 108306370 intron variant T/A;C snv 3
rs3827760
RANBP2 ; EDAR
0.752 0.160 2 108897145 missense variant A/G snv 0.15 5.9E-02 5
rs3184504
SH2B3 ; ATXN2
0.572 0.600 12 111446804 missense variant T/A;C;G snv 0.67 29
rs397507546
PTPN11
0.790 0.360 12 112489084 missense variant G/A;C;T snv 2
rs7086803
VTI1A
0.763 0.160 10 112738717 intron variant G/A snv 0.20 8
rs121913331
APC
0.851 0.120 5 112838934 stop gained C/A;T snv 8.0E-06 6
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 7
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 38
rs26538
ATG12 ; AP3S1
1.000 0.040 5 115842698 intron variant C/T snv 0.44 1
rs1484038087
ROS1
1.000 0.040 6 117317181 missense variant C/T snv 4.0E-06 1
rs1057519788
ROS1
0.925 0.080 6 117317184 missense variant C/T snv 5
rs6942067
DCBLD1
1.000 0.040 6 117464533 intron variant A/G snv 0.38 1
rs9387478
DCBLD1
0.851 0.080 6 117465017 intron variant C/A;T snv 3
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
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 2
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 2
rs11200014
FGFR2
0.695 0.280 10 121575416 intron variant G/A;T snv 0.34 3
rs754284524
SRFBP1 ; LOX
1.000 0.040 5 122074125 stop gained -/TACATGCTAGATTCATTTTAACTCAATACTGCCATTCAATTCTAGCAAC ins 4.0E-06 2