Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs3865014
GLCE
0.851 0.080 15 69269179 missense variant G/A snv 0.75 0.69 8
rs4849887 0.807 0.080 2 120487546 intergenic variant T/A;C snv 7
rs4415084 0.827 0.080 5 44662413 upstream gene variant C/T snv 0.49 6
rs10771399 0.827 0.080 12 28002147 intergenic variant A/G snv 8.9E-02 5
rs1064793184
FBXO11 ; MSH6
0.851 0.080 2 47791055 missense variant A/G snv 4
rs1114167795
FBXO11 ; MSH6
0.851 0.080 2 47799482 missense variant C/T snv 4
rs12662670
CCDC170
0.851 0.080 6 151597721 intron variant T/C;G snv 4
rs13000023
LOC101928278 ; LOC105373873
0.851 0.080 2 217059671 downstream gene variant G/A;C;T snv 0.19 4
rs142030651
EP300
0.851 0.080 22 41117723 missense variant G/A;C snv 6.1E-03 4
rs1436904
AQP4-AS1 ; CHST9
0.851 0.080 18 26990703 intron variant T/G snv 0.35 4
rs1485579458
ERBB2
0.851 0.080 17 39723921 missense variant A/G snv 4.0E-06 4
rs1726801
POLD1
0.851 0.080 19 50401817 missense variant G/A snv 0.11 0.14 4
rs373587423
ERCC4
0.851 0.080 16 13935425 missense variant T/C snv 3.6E-05 7.0E-06 4
rs4986850
BRCA1
0.851 0.080 17 43093454 missense variant C/A;T snv 5.8E-02 4
rs527616
AQP4-AS1
0.851 0.080 18 26757460 intron variant C/G snv 0.71 4
rs564064363
ERBB2
0.851 0.080 17 39706998 missense variant G/A;C snv 1.3E-05 4
rs1235679626
MORC2
0.925 0.080 22 30940834 missense variant C/T snv 1.4E-05 3
rs769483475
CD44
0.925 0.080 11 35229231 missense variant G/A snv 8.0E-06 3
rs780439043
EGFR
0.925 0.080 7 55205301 missense variant A/G snv 8.0E-06 1.4E-05 3
rs10274701
EZH2
0.925 0.080 7 148855364 intron variant C/T snv 0.76 2
rs1064793309
BRCA1
0.925 0.080 17 43063889 missense variant C/T snv 2
rs148047459
MUL1
0.925 0.080 1 20501166 missense variant G/A snv 8.0E-06 2.1E-05 2
rs1651654
C16orf87
0.925 0.080 16 46822677 intron variant T/C snv 0.79 2
rs184967
MSH3
0.925 0.080 5 80854162 missense variant A/G;T snv 0.87 2
rs2077197
PARP1
0.925 0.080 1 226408338 upstream gene variant C/G;T snv 2