Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs397514606
AKT3
0.763 0.320 1 243695714 missense variant C/T snv 14
rs121913396
CTNNB1
0.732 0.200 3 41224607 missense variant A/C;G;T snv 13
rs121913357
BRAF
0.742 0.320 7 140781603 stop gained C/A;G;T snv 12
rs121913366
BRAF
0.763 0.400 7 140753345 missense variant A/C;T snv 12
rs121913407
CTNNB1
0.763 0.240 3 41224645 missense variant T/C;G snv 12
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
rs3088440
CDKN2A ; CDKN2A-DT
0.776 0.240 9 21968160 3 prime UTR variant G/A snv 0.13 12
rs1057519855
HRAS ; LRRC56
0.776 0.120 11 533873 missense variant CT/AC;TC mnv 11
rs11225395
MMP8
0.776 0.360 11 102725749 intron variant A/C;G snv 11
rs121913378
BRAF
0.776 0.280 7 140753337 missense variant C/A;G;T snv 11
rs121913492
GNAQ
0.790 0.160 9 77794572 missense variant T/A;C;G snv 11
rs397516896
BRAF
0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs121913365
BRAF
0.776 0.320 7 140753332 missense variant T/A;G snv 10
rs121913370
BRAF
0.763 0.360 7 140753393 missense variant T/C;G snv 10
rs121913513
KIT
0.776 0.120 4 54727495 missense variant T/C snv 10
rs397507484
BRAF
0.752 0.480 7 140753333 missense variant T/A;C;G snv 10
rs4516035
VDR
0.776 0.360 12 47906043 non coding transcript exon variant T/C snv 0.31 10
rs6059655
RALY
0.790 0.080 20 34077942 intron variant A/G snv 0.95 10
rs1057519874
RAC1
0.807 0.120 7 6387261 missense variant C/A;T snv 9
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 9
rs193922219
FBN1
0.763 0.280 15 48446701 splice region variant C/A;T snv 9
rs3024493
IL19 ; IL10
0.776 0.280 1 206770623 intron variant C/A;T snv 0.11 9
rs7023329
MTAP
0.790 0.160 9 21816529 intron variant A/G snv 0.50 9
rs869025608
MAP2K1
0.763 0.400 15 66435117 missense variant G/C;T snv 9