Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
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
rs3735485
MYO1G
7 44969742 missense variant A/G snv 0.87 0.88 6
rs9400271
CCDC162P
6 109286353 non coding transcript exon variant G/A snv 0.51 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
rs10858740 12 88451258 intergenic variant A/G;T snv 0.56 5
rs114050631 2 218156235 regulatory region variant C/T snv 6.9E-03 5
rs1144700
ATXN1
6 16744456 intron variant C/G;T snv 5
rs11624512
RIN3
14 92644775 non coding transcript exon variant C/T snv 0.15 5
rs11654074
VMP1
17 59748211 intron variant A/C snv 0.40 5
rs11725704 4 74094279 downstream gene variant A/G snv 0.28 5
rs12542907 8 67900953 intergenic variant C/G snv 0.29 5
rs12550612
TNFRSF10C
8 23109256 intron variant G/A snv 0.83 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
rs146890554
CSF3
17 40017384 3 prime UTR variant C/T snv 9.6E-03 5
rs147694761
NPC1
18 23571654 intron variant AAAA/-;A;AA;AAA;AAAAA;AAAAAA delins 5
rs16850073
CXCL6
4 73838282 3 prime UTR variant C/T snv 0.29 5
rs16978075
LINC01478 ; LINC01601
18 44533186 intron variant T/C snv 8.5E-02 5
rs192022
C11orf65
11 108378047 intron variant C/G;T snv 5
rs1968252
LOC105372263
19 7782850 upstream gene variant G/A;T snv 5