Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11255841 0.776 0.080 10 8697617 intergenic variant T/A snv 0.25 11
rs719725 0.827 0.080 9 6365683 intergenic variant A/C snv 0.34 7
rs1535989 0.925 0.080 13 105370372 intergenic variant A/G;T snv 4
rs3789243
ABCB1
0.776 0.120 7 87591570 intron variant A/G snv 0.50 14
rs104894194
AIP
0.925 11 67483198 stop gained C/T snv 2.8E-05 2.1E-05 4
rs2276020
AIP ; MIR6752
1.000 0.120 11 67490085 missense variant C/G;T snv 3.4E-02 2
rs10941112
AMACR ; C1QTNF3-AMACR
0.882 0.120 5 34004602 missense variant C/T snv 0.42 0.38 4
rs1800497
ANKK1
0.620 0.400 11 113400106 missense variant G/A snv 0.26 0.26 56
rs1801155
APC
0.649 0.440 5 112839514 missense variant T/A snv 8.0E-06; 2.0E-03 1.2E-03 42
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs1801166
APC
0.732 0.200 5 112839543 missense variant G/C snv 4.4E-03 5.6E-03 17
rs459552
APC
0.752 0.320 5 112841059 missense variant T/A;G snv 0.79 14
rs1268298845
APC
0.882 0.120 5 112780878 missense variant G/A snv 4.0E-06 4
rs17503908
ATM ; C11orf65
1.000 0.080 11 108344670 intron variant T/G snv 6.7E-02 2
rs113488022
BRAF
0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs386834263
CACNA1D
3 53673113 missense variant G/C snv 1
rs10505477
CASC8 ; PCAT1 ; POU5F1B
0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs7837328
CASC8 ; PCAT1 ; POU5F1B
0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs5443
CDCA3 ; GNB3
0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 106
rs3802842
COLCA2 ; COLCA1
0.695 0.280 11 111300984 intron variant C/A snv 0.71 25
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1130864
CRP
0.672 0.520 1 159713301 3 prime UTR variant G/A snv 0.26 27
rs774679649
CRP
1 159713878 missense variant T/C snv 4.0E-06 7.0E-06 1
rs121913409
CTNNB1
0.708 0.400 3 41224646 missense variant C/A;G;T snv 21