Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9581943
PDX1
1.000 0.120 13 27919860 upstream gene variant G/A snv 0.31 1
rs2900174
PRB2 ; PRB1
1.000 0.120 12 11394598 intron variant A/G snv 0.12 1
rs121912576
SMAD4
1.000 0.120 18 51065539 stop gained G/T snv 1
rs121912578
SMAD4
1.000 0.120 18 51078285 missense variant G/C snv 1
rs121912579
SMAD4
1.000 0.120 18 51078351 stop gained A/T snv 1
rs2417487
SMC2
1.000 0.120 9 104125300 intron variant A/G;T snv 1
rs375328708
STK11
1.000 0.120 19 1226602 synonymous variant C/G;T snv 6.7E-05 6.3E-05 1
rs397518442
STK11
1.000 0.120 19 1220630 frameshift variant C/- delins 1
rs17688601
SUGCT ; LOC112267984
1.000 0.120 7 40827064 intron variant C/A snv 0.20 1
rs200027650
TCHP
1.000 0.120 12 109904025 missense variant G/A snv 2.5E-04 1.4E-04 1
rs73328514
TNS3
1.000 0.120 7 47448971 intron variant A/T snv 0.15 1
rs77038344
TNS4
1.000 0.120 17 40487962 intron variant C/T snv 8.4E-02 1
rs121912661
TP53
1.000 0.120 17 7676264 missense variant C/A;G snv 1
rs351365
WNT2B
1.000 0.120 1 112503773 intron variant T/C;G snv 1
rs4285214
ZNF608
1.000 0.120 5 124688588 intron variant T/G snv 0.55 1
rs16986825
ZNRF3
1.000 0.120 22 28904318 intron variant C/T snv 0.13 1
rs10887710 0.925 0.120 10 80270029 downstream gene variant T/C snv 0.19 2
rs10919791 0.925 0.240 1 199996040 intergenic variant G/A snv 0.22 2
rs1552462 0.925 0.120 11 7235910 upstream gene variant C/T snv 2.7E-02 2
rs2816938 1.000 0.120 1 200016240 upstream gene variant T/A snv 0.37 2
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs9573163 0.925 0.120 13 73334709 regulatory region variant C/G;T snv 2
rs708224
BICD1
0.925 0.120 12 32283475 intron variant A/G snv 0.50 2
rs11644043
BRD7
0.925 0.120 16 50327466 intron variant T/C snv 0.24 2
rs782128510
C17orf97 ; LOC105371430
0.925 0.120 17 410373 missense variant C/A;G snv 7.6E-05; 8.4E-06 2