Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs401681
CLPTM1L
0.620 0.640 5 1321972 intron variant C/T snv 0.48 42
rs9420907
STN1
0.790 0.320 10 103916707 intron variant C/A;G snv 7
rs1561927
LINC00824
0.807 0.280 8 128555832 intron variant C/T snv 0.65 6
rs11125529
ACYP2
0.882 0.280 2 54248729 intron variant C/A;T snv 3
rs9854771
TP63
0.925 0.240 3 189790682 intron variant G/A snv 0.34 2
rs1719217
LOC102724850
1.000 0.120 17 36080352 intron variant T/A;G snv 1
rs7779540
DPP6
1.000 0.120 7 153925577 intron variant G/A snv 6.7E-02 1
rs7675998 0.827 0.360 4 163086668 intergenic variant A/G;T snv 5
rs10919791 0.925 0.240 1 199996040 intergenic variant G/A snv 0.22 2
rs11571833
BRCA2
0.608 0.360 13 32398489 stop gained A/T snv 6.6E-03 6.0E-03 43
rs80358972
BRCA2
0.742 0.480 13 32356472 stop gained C/A;T snv 8.0E-06; 3.2E-05 12
rs1569119395
WNT7B
0.925 0.120 22 45949926 stop gained G/A snv 2
rs397518481
RARB
0.925 0.120 3 25501230 stop gained C/G;T snv 2
rs267607096
STRA6
1.000 0.120 15 74202199 stop gained C/T snv 5.6E-06 1
rs121913529
KRAS
0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913530
KRAS
0.583 0.640 12 25245351 missense variant C/A;G;T snv 63
rs762846821
TP53
0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs17879961
CHEK2
0.597 0.480 22 28725099 missense variant A/C;G snv 4.1E-03 53
rs1444669684
CDKN2B-AS1 ; CDKN2A
0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs121913495
GNAS
0.672 0.400 20 58909366 missense variant G/A;T snv 28
rs6136
SELP
0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 17
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs746284240
MDM2
0.763 0.240 12 68809243 missense variant A/G snv 11
rs1037189404
MUC1
0.776 0.280 1 155187519 missense variant C/T snv 8
rs121909235
PTEN
0.851 0.240 10 87957919 missense variant G/A snv 8