Source: INFERRED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894229
LRRC56 ; HRAS
0.564 0.600 11 534289 missense variant C/A;G;T snv 52
rs104894230
HRAS ; LRRC56
0.564 0.600 11 534288 missense variant C/A;G;T snv 36
rs104886003
PIK3CA
0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 34
rs121913274
PIK3CA
0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs397516436
TP53
0.641 0.440 17 7674894 stop gained G/A;C snv 26
rs11554290
NRAS
0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs121913275
PIK3CA
0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs138729528
TP53
0.677 0.480 17 7675089 missense variant G/A;C snv 1.6E-05 25
rs587778720
TP53
0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs121913255
NRAS
0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs753660142
TP53
0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs121912660
TP53
0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs1057519045
FGFR2
0.851 0.160 10 121498522 missense variant T/G snv 6
rs1063192
CDKN2B ; CDKN2B-AS1
0.695 0.520 9 22003368 3 prime UTR variant G/A;T snv 6
rs1057519854
FGFR2
0.882 0.080 10 121488063 missense variant A/T snv 5
rs1057519901
FGFR2
0.925 0.080 10 121498525 missense variant T/G snv 5
rs121913476
FGFR2
0.851 0.080 10 121498520 missense variant A/C;T snv 5
rs2517713
HLA-A
1.000 0.120 6 29950322 downstream gene variant G/A;T snv 2
rs2860580
HLA-A
1.000 0.120 6 29938914 upstream gene variant A/C;G;T snv 2
rs180177133
PALB2
0.807 0.240 16 23614089 frameshift variant T/- delins 1.2E-05 1.4E-05 9
rs28421666 1.000 0.120 6 32624960 upstream gene variant A/G snv 6.9E-02 2
rs189897
ITGA9
1.000 0.120 3 37477054 intron variant T/A snv 0.13 2
rs17111237
CEP128
14 80939997 intron variant A/G snv 0.15 1
rs9510787
TNFRSF19
1.000 0.120 13 23631056 intron variant A/G snv 0.20 2
rs2894207
LINC02571 ; HLA-B
0.882 0.160 6 31295974 intron variant T/C snv 0.20 7