Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs13181
KLC3 ; ERCC2
0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs187238
IL18
0.602 0.680 11 112164265 intron variant C/A;G snv 48
rs180177035
BRAF
0.752 0.280 7 140801502 missense variant T/C snv 35
rs104894226
LRRC56 ; HRAS
0.658 0.560 11 534285 missense variant C/A;G;T snv 29
rs2294020
CCDC22
0.763 0.280 X 49246763 missense variant A/G;T snv 10
rs5934505 0.776 0.120 X 8945785 intergenic variant T/A;C snv 10
rs1057517491
GJB2
0.776 0.240 13 20189448 frameshift variant C/- delins 8
rs10888690
FAF1
0.807 0.080 1 50494849 intron variant T/A;C snv 7
rs10930758 0.807 0.080 2 176897100 intergenic variant A/G;T snv 7
rs11037975 0.807 0.080 11 44389312 intergenic variant C/A;G snv 7
rs13405699 0.807 0.080 2 173740905 intergenic variant C/A;G;T snv 7
rs2095921
C1orf127
0.807 0.080 1 10973265 intron variant C/G;T snv 7
rs246180 0.807 0.080 16 14298066 upstream gene variant C/A;T snv 7
rs34991987
LOC105375343
0.807 0.080 7 69130240 downstream gene variant A/-;AA delins 7
rs3781458
FAM53B
0.807 0.080 10 124655362 intron variant C/A;G;T snv 7
rs4679956
LOC107986047
0.807 0.080 3 151937074 intergenic variant C/A;T snv 7
rs71421546
LOC100129455 ; HOXD-AS2
0.807 0.080 2 176127129 intron variant C/A;T snv 7
rs72561723
GJB2
0.790 0.240 13 20189448 missense variant C/T snv 8.0E-06 7
rs7349332
WNT10A
0.807 0.080 2 218891661 intron variant C/G;T snv 7
rs7534070 0.807 0.080 1 25171684 intergenic variant G/A;T snv 7
rs7801037
HDAC9
0.807 0.080 7 18857888 intron variant C/A;G;T snv 7
rs7974900
LOC105369705 ; SSPN ; LOC105369704
0.807 0.080 12 26275744 intron variant T/A;C snv 7
rs8085664
SLC14A2
0.807 0.080 18 45234191 intron variant C/A;T snv 7
rs9357047 0.807 0.080 6 9327323 intergenic variant T/A;C snv 7
rs9719620
MKLN1-AS ; MKLN1
0.807 0.080 7 131309621 non coding transcript exon variant T/A;C snv 7