Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519949
RHEB
0.851 0.120 7 151490964 missense variant A/T snv 6
rs798766
TACC3
0.851 0.120 4 1732512 intron variant T/C snv 0.76 6
rs1367215622
PHLPP2
1.000 0.120 16 71714618 missense variant A/C snv 4.0E-06 2
rs750802459
CASP3
1.000 0.120 4 184635342 frameshift variant TCAGGATAATCCATTTTATAACTGTTGTCCAGGGATATTCCAGAGTC/- delins 5.6E-05 2
rs1057519780
MTOR
1.000 0.120 1 11127800 missense variant C/T snv 1
rs142548892
SFXN1
1.000 0.120 5 175509071 missense variant G/A;T snv 1.2E-05; 4.0E-06 1
rs4987853
BCL2
1.000 0.120 18 63126422 3 prime UTR variant T/C;G snv 0.23 1
rs587777900
MTOR
1.000 0.120 1 11114363 missense variant C/T snv 1
rs1057519911
MAPK1
0.776 0.160 22 21772875 missense variant C/T snv 10
rs1057519893
ERBB3
0.790 0.160 12 56085070 missense variant G/A;T snv 9
rs759610249
FBXW7
0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs786201419
TP53
0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs1057519920
NFE2L2
0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs121913468
ERBB2
0.827 0.160 17 39724008 missense variant G/A;C;T snv 7
rs1057519732
MAP2K1
0.827 0.160 15 66436824 missense variant C/A;T snv 6
rs1057519891
ERBB3
0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06 6
rs1057519931
PIK3CA
0.827 0.160 3 179199141 missense variant G/C snv 6
rs1057519862
ERBB2
0.851 0.160 17 39723405 missense variant G/A snv 5
rs1057519892
ERBB3
0.851 0.160 12 56088558 missense variant A/T snv 5
rs28931588
CTNNB1
0.701 0.200 3 41224606 missense variant G/A;C;T snv 17
rs1057519816
ERBB2
0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs121913228
CTNNB1
0.742 0.200 3 41224621 missense variant T/C;G snv 14
rs1057519940
PIK3CA
0.752 0.200 3 179218308 missense variant G/T snv 13
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs121913470
ERBB2
0.776 0.200 17 39723967 missense variant T/C;G snv 13