Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1371429276
PTPRT
1.000 0.080 20 42472359 missense variant G/A snv 1.4E-05 1
rs63749803
MLH1
1.000 0.080 3 37004421 missense variant T/C;G snv 1
rs63750297
MLH1
1.000 0.080 3 37004412 missense variant C/A;G;T snv 8.0E-06 1
rs63750795
MSH2
1.000 0.080 2 47480854 missense variant T/G snv 1
rs63750966
MSH2
1.000 0.080 2 47403240 missense variant G/A;C;T snv 1
rs63751047
MLH1
1.000 0.080 3 37048525 missense variant C/A;G snv 1
rs63751400
MSH2
1.000 0.080 2 47480839 missense variant C/G;T snv 4.0E-06 1
rs747093473
CDX2
1.000 0.080 13 27968819 missense variant G/A snv 7.0E-06 1
rs768678989
MET
1.000 0.080 7 116771932 missense variant C/T snv 2.8E-05 1
rs771333219
MET
1.000 0.080 7 116759444 missense variant C/T snv 1.2E-04 8.4E-05 1
rs780759537
CDH1
1.000 0.080 16 68822082 missense variant G/A snv 1.6E-05 4.2E-05 1
rs2269772
ITGA3
0.925 0.080 17 50072022 synonymous variant C/T snv 0.17 0.19 6
rs11187842
PLCE1
0.925 0.080 10 94292754 intron variant C/T snv 7.8E-02 5
rs2070803
TRIM46
0.925 0.080 1 155185239 intron variant G/A snv 0.55 5
rs11869286
STARD3
0.925 0.080 17 39657603 intron variant G/C snv 0.52 4
rs1305398818
ABCG2
0.925 0.080 4 88131886 missense variant G/A;C snv 4.0E-06; 4.0E-06 4
rs6087990
DNMT3B
0.925 0.080 20 32762102 upstream gene variant T/C;G snv 4
rs63750623
MSH2
0.925 0.160 2 47480707 stop gained C/G;T snv 4
rs6733301
EFR3B
0.925 0.080 2 25053415 intron variant G/A snv 0.13 4
rs8193
CD44
0.925 0.080 11 35229771 3 prime UTR variant C/T snv 0.29 4
rs881844
STARD3
0.925 0.080 17 39653965 intron variant C/G snv 0.51 4
rs9589207
MIR17HG ; MIR92A1 ; MIR19B1 ; MIR20A ; MIR19A
0.925 0.080 13 91351335 mature miRNA variant G/A;C snv 5.4E-03; 4.0E-06 4
rs9972882
STARD3
0.925 0.080 17 39651445 intron variant A/C snv 0.66 4
rs1064261
MTOR
0.925 0.080 1 11228701 missense variant G/A;T snv 0.75; 4.0E-06 3
rs111638916
PSMD10
0.925 0.080 X 108084839 3 prime UTR variant G/A snv 3