Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12520522 5 40494576 intron variant C/A;G;T snv 1
rs17636351 12 59216246 intergenic variant C/G;T snv 1
rs2326451 6 126490782 intron variant A/T snv 0.44 1
rs554093579 7 100537063 upstream gene variant A/C snv 5.5E-03 1
rs75225321 16 89672182 non coding transcript exon variant G/- del 0.23 1
rs6430549
ACMSD ; CCNT2-AS1
2 134858776 intron variant A/G snv 0.58 1
rs10953299
ACTL6B
7 100645788 intron variant T/C snv 0.21 1
rs7311607
CACNA1C
12 2413815 intron variant A/G snv 0.34 1
rs8100454
CYP2F2P
19 40820613 intron variant A/G snv 9.7E-02 1
rs8108461
DOT1L
19 2186758 intron variant T/C snv 0.55 1
rs576195416
EGLN1
1 231374522 intron variant TT/-;T;TTT;TTTT;TTTTTTTTTTTT delins 1
rs17400517
FCGR2A
1 161515469 intron variant G/T snv 8.5E-02 1
rs111843364
HYDIN
16 70923707 intron variant G/A snv 3.8E-02 1
rs150522999
LINC00894
X 150167578 intron variant C/G snv 5.0E-02 1
rs73736914
LOC101929705
6 44010849 intron variant A/G snv 3.6E-02 1
rs9273039
LOC107986589 ; HLA-DQA1
6 32644174 non coding transcript exon variant C/A;T snv 1
rs151165225
MARK4
19 45257662 intron variant C/T snv 0.19 1
rs10711289
MECOM ; MECOM-AS1
3 169450583 intron variant AAA/-;A;AA;AAAA;AAAAA delins 1
rs138308793
MIR4435-2HG ; SOCAR
2 111493181 intron variant G/A snv 0.11 1
rs6442310
PPARG
3 12316731 intron variant T/A snv 0.66 1
rs145611121
PRDM16
1 3402268 intron variant -/C;CC delins 1
rs552708909
PRRG2 ; NOSIP
19 49587166 intron variant T/-;TT;TTT delins 1
rs7563124
PSD4
2 113207621 3 prime UTR variant T/A snv 0.27 1
rs12548864
PVT1
8 127916000 intron variant C/T snv 0.27 1
rs143985986
PXK
3 58414160 3 prime UTR variant C/- del 0.25 1