Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2038700
STXBP6
14 24992783 intron variant T/C snv 0.53 7
rs2249742
HLA-B ; HLA-C
0.925 0.120 6 31272944 intron variant C/T snv 0.50 7
rs333947
CSF1
1 109928142 intron variant G/A snv 0.13 7
rs342293
CTB-30L5.1
0.882 0.040 7 106731773 intron variant C/G snv 0.42 7
rs6795735
ADAMTS9-AS2
0.882 0.120 3 64719689 intron variant C/A;G;T snv 7
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs3755967
GC
0.925 0.080 4 71743681 intron variant C/A;T snv 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs7740107
L3MBTL3
1.000 0.080 6 130053316 intron variant T/A;G snv 6
rs10075801
MIR3936HG ; SLC22A4
5 132341949 intron variant A/G snv 0.31 5
rs10138752
RAD51B
14 68713254 intron variant C/T snv 8.8E-02 5
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11970772
CCND3
6 41957552 intron variant T/A snv 0.24 5
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 5
rs13063578
SETD2
3 47046347 intron variant T/A snv 0.46 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
rs1512282
LOC105377462
4 144510345 intron variant A/C;G snv 0.33 5
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02 5
rs2022003
SPTA1
1 158617176 intron variant A/T snv 0.28 5
rs2075302
FAP
0.882 2 162219636 intron variant T/C snv 0.34 5
rs2158799
JAZF1-AS1
7 28237488 intron variant C/G;T snv 0.70 5
rs238914
ZBTB16
11 114113387 intron variant C/A snv 0.45 5