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
rs3024971
STAT6
0.827 0.200 12 57099944 intron variant T/G snv 7.8E-02 7.9E-02 7
rs3731211
CDKN2A
9 21986848 intron variant T/A snv 0.74 7
rs60600003
ELMO1
0.827 0.120 7 37342861 intron variant T/C;G snv 7
rs8129030
RUNX1
0.807 0.120 21 35340290 intron variant T/A;G snv 0.72 7
rs10774624
LINC02356
0.882 0.160 12 111395984 intron variant G/A snv 0.67 6
rs16917546
LOC105378327 ; ZNF365
0.851 0.040 10 62637778 intron variant T/C snv 0.29 6
rs2524079
HLA-B
6 31274397 intron variant G/A snv 0.44 6
rs2979489
RBPMS
8 30423317 intron variant G/A;C snv 6
rs34208856
HBS1L
6 135099930 intron variant TT/-;T;TTT;TTTTTTTTT delins 6
rs4821544
NCF4-AS1 ; NCF4
0.925 0.040 22 36862461 intron variant T/A;C snv 6
rs726657
DELEC1
0.827 0.120 9 114934056 intron variant C/T snv 0.50 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
rs10173538
BAZ2B ; MARCHF7
2 159712765 intron variant C/G;T snv 5
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 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
rs16978075
LINC01478 ; LINC01601
18 44533186 intron variant T/C snv 8.5E-02 5
rs17445836 0.851 0.320 16 85984057 intron variant G/A snv 0.15 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs1982094
CCDC26
8 129612570 intron variant C/T snv 4.8E-02 5