Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913377
BRAF
0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs28934872
TSC2
0.851 0.200 16 2070571 missense variant G/A snv 5
rs45469298
TSC2
0.851 0.200 16 2070570 missense variant C/G;T snv 5
rs45517305
TSC2
0.851 0.240 16 2081646 stop gained C/A;T snv 5
rs118203542
TSC1
0.851 0.200 9 132906053 stop gained G/A snv 4
rs118203631
TSC1
0.851 0.200 9 132903785 stop gained G/A snv 4
rs118203434
TSC1
0.925 0.120 9 132921367 stop gained G/A snv 3
rs137854218
TSC2 ; PKD1
0.925 0.120 16 2088293 inframe insertion CATCAAGCGGCTCCGCCA/-;CATCAAGCGGCTCCGCCACATCAAGCGGCTCCGCCA delins 3
rs45507199
TSC2 ; PKD1
0.925 0.120 16 2088294 missense variant G/A;C;T snv 3
rs45517259
TSC2
0.925 0.120 16 2076142 missense variant G/A snv 3
rs1060500931
TSC2
0.925 0.120 16 2064302 stop gained C/T snv 2
rs1064794132
TSC1
1.000 0.120 9 132903649 splice donor variant A/T snv 2
rs1114167462
TSC2
1.000 0.120 16 2062533 stop gained C/T snv 2
rs118203673
TSC1
0.925 0.160 9 132902703 stop gained G/A snv 2
rs1567533189
TSC2
0.925 0.160 16 2086283 frameshift variant AAGGACTGCCA/- del 2
rs397514914
TSC2
1.000 0.120 16 2071534 missense variant C/T snv 2
rs397514916
TSC2
0.925 0.120 16 2083754 missense variant C/G;T snv 2
rs45438205
TSC2
0.925 0.120 16 2080365 missense variant C/T snv 7.0E-06 2
rs45483392
TSC2
0.925 0.120 16 2087897 missense variant C/A;T snv 2
rs45487497
TSC2
0.925 0.120 16 2058779 missense variant G/A snv 2
rs45516293
TSC2
0.925 0.120 16 2084965 missense variant A/C;G snv 2
rs45517169
TSC2
0.925 0.120 16 2062982 stop gained C/T snv 2
rs45517234
TSC2
0.925 0.160 16 2074251 stop gained C/T snv 2
rs45517258
TSC2
0.925 0.120 16 2076141 missense variant C/G;T snv 2
rs45517382
TSC2
0.925 0.120 16 2086834 missense variant A/G snv 2