Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2647087 1.000 0.040 6 32713272 upstream gene variant A/C snv 0.29 2
rs4437130 1.000 0.040 3 2035283 intergenic variant G/A snv 0.12 2
rs62561366 1.000 0.040 9 95555669 intergenic variant A/T snv 3.9E-02 2
rs379742 1.000 0.040 X 106250703 intergenic variant G/A snv 0.17 1
rs698
ADH1C ; ADH1B
0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs574363219
APOA5 ; ZPR1
1.000 0.040 11 116790427 missense variant C/T snv 1.4E-04 2
rs140808909
APOE
0.851 0.120 19 44909080 missense variant G/A snv 2.0E-04 5.6E-05 5
rs190853081
APOE
0.925 0.080 19 44909083 missense variant G/A snv 2.0E-04 5.6E-05 3
rs1335550286
APOE
1.000 0.040 19 44909005 missense variant G/A snv 7.0E-06 2
rs1801725
CASR
0.633 0.600 3 122284910 missense variant G/T snv 0.13 0.11 39
rs1042636
CASR
0.672 0.360 3 122284922 missense variant A/G snv 0.15 9.0E-02 23
rs1801726
CASR
0.732 0.280 3 122284985 missense variant G/C snv 0.95 0.92 13
rs756322971
CASR
0.763 0.240 3 122284955 missense variant C/A;G snv 9
rs1800076
CFTR
0.763 0.200 7 117509093 missense variant G/A;T snv 1.5E-02; 8.0E-06 10
rs76371115
CFTR
0.807 0.160 7 117531041 missense variant A/C;G;T snv 8.0E-06 6
rs397508687
CFTR
0.827 0.080 7 117531040 frameshift variant -/GA ins 4.0E-06 5
rs11971167
CFTR
0.882 0.160 7 117642528 missense variant G/A;T snv 1.3E-03 3
rs397508139
CFTR
0.882 0.160 7 117540237 missense variant T/A;C snv 4.0E-06; 4.0E-06 3
rs772223589
CFTR
0.925 0.120 7 117590391 missense variant C/G;T snv 4.0E-06; 1.2E-05 3
rs74571530
CFTR ; CFTR-AS1
0.882 0.160 7 117559594 missense variant T/A;C;G snv 9.4E-04 3
rs199695765
CPA2
0.925 0.160 7 130269008 stop gained C/T snv 8.8E-05 1.3E-04 2
rs777418530
CRISPLD2
0.763 0.120 16 84845883 missense variant A/G snv 4.0E-06 7.0E-06 10
rs775437927
CRISPLD2
0.882 0.080 16 84849390 missense variant G/A snv 6.0E-05 7.0E-06 3
rs1451011538
CRISPLD2
0.925 0.080 16 84838647 missense variant T/A snv 4.0E-06 2
rs121909293
CTRC
0.851 0.080 1 15445717 missense variant C/T snv 4.4E-03 3.8E-03 5