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
rs2736100
TERT
0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 59
rs6025
F5
0.637 0.560 1 169549811 missense variant C/T snv 1.8E-02 43
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs1463038513
APC
0.658 0.440 5 112839511 frameshift variant TAAA/- delins 36
rs74315401
PRNP
0.683 0.320 20 4699525 missense variant C/T snv 32
rs165599
ARVCF ; COMT
0.677 0.280 22 19969258 3 prime UTR variant G/A snv 0.56 27
rs2104286
IL2RA
0.662 0.440 10 6057082 intron variant T/C snv 0.18 25
rs3803662
CASC16
0.662 0.440 16 52552429 non coding transcript exon variant A/G snv 0.63 25
rs4939827
SMAD7
0.708 0.160 18 48927093 intron variant T/A;C snv 25
rs63750231
PSEN1
0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs104893878
SNCA ; SNCA-AS1
0.732 0.160 4 89835580 missense variant C/G snv 21
rs28931614
FGFR3
0.672 0.520 4 1804392 missense variant G/A;C snv 21
rs2981582
FGFR2
0.695 0.360 10 121592803 intron variant A/G snv 0.58 21
rs1475170339
IGFALS ; SPSB3
0.732 0.240 16 1792325 missense variant T/C;G snv 18
rs267607165
TUBB3
0.708 0.520 16 89935679 missense variant G/A;C snv 18
rs1219648
FGFR2
0.716 0.320 10 121586676 intron variant A/G;T snv 17
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 17
rs13387042
LOC105373874 ; LOC101928278
0.732 0.280 2 217041109 intergenic variant A/G snv 0.44 16
rs63751438
MAPT
0.776 0.120 17 46010388 missense variant C/T snv 16
rs10993994
MSMB
0.763 0.280 10 46046326 5 prime UTR variant A/G snv 0.54 15
rs121918075
TTR
0.752 0.280 18 31598632 missense variant A/G snv 15
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 15
rs965513
PTCSC2
0.742 0.200 9 97793827 intron variant A/G;T snv 15