Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs12600856 17 40007042 intergenic variant T/C;G snv 5
rs139707092
SPC25 ; NOSTRIN
2 168850753 intron variant TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT delins 5
rs145013566
PNKD
2 218297998 intron variant -/C ins 5
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs1968252
LOC105372263
19 7782850 upstream gene variant G/A;T snv 5
rs201950044 1 161639782 intergenic variant G/T snv 5
rs2208568
LOC105373215 ; LINC02768
1 235926855 intergenic variant T/A;C;G snv 5
rs2416257
WDR36
0.882 0.160 5 111099792 intron variant C/G;T snv 5
rs34061361
FLT3
13 28044450 intron variant AAA/-;A;AA;AAAA delins 5
rs3917914
CSF3R
1 36482287 intron variant G/A;T snv 5
rs397731840
CCDC26
8 129599504 intron variant TT/-;T;TTT;TTTT;TTTTT delins 5
rs397933924 10 97314229 upstream gene variant -/CAGGTTCAAGCGA ins 5
rs6500550
TRAP1
16 3696240 intron variant C/G;T snv 5
rs66505542
BUD13
11 116752498 intron variant AA/-;A;AAA delins 5
rs73316435
ITGB3
0.882 17 47252111 upstream gene variant C/A;T snv 5
rs8705
ETS1
11 128459018 3 prime UTR variant G/A;T snv 5
rs960709
TNIP1
0.882 0.120 5 151081488 intron variant A/G;T snv 5
rs9979383
RUNX1
0.925 0.200 21 35343463 intron variant C/G;T snv 5
rs10206089 2 61476184 intron variant G/A snv 4
rs10795656 1.000 0.080 10 8553876 intergenic variant G/A;T snv 4
rs10905284
GATA3
0.882 0.200 10 8073399 intron variant C/A;T snv 4
rs11204682
ENSA
1 150623061 intron variant G/A;T snv 4
rs11405616
NDFIP1
5 142130697 intron variant A/-;AA;AAA;AAAA delins 4