Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs17630235
TRAFD1
0.925 0.120 12 112153882 downstream gene variant G/A;C snv 7
rs198846
H1-6
6 26107235 downstream gene variant A/G;T snv 7
rs881858
LOC105375069 ; LOC107986598
0.882 0.200 6 43838872 intron variant G/A;C snv 7
rs8887
PLIN4 ; HDGFL2
1.000 0.080 19 4502189 3 prime UTR variant T/C;G snv 0.51; 1.8E-05 7
rs9349205
CCND3
6 41957421 intron variant G/A;C snv 7
rs1256030
ESR2
0.827 0.240 14 64280452 intron variant A/G;T snv 6
rs4886755
NRG4
0.925 0.120 15 76005791 non coding transcript exon variant A/G;T snv 0.49 6
rs615672
HLA-DRB1
0.851 0.240 6 32606394 intergenic variant G/A;C snv 6
rs707889
HFE
0.827 0.200 6 26095703 3 prime UTR variant G/A;T snv 6
rs729761
LOC105375069 ; LOC107986598
0.925 0.120 6 43836834 intron variant T/A;G snv 6
rs7753826 0.925 0.120 6 26042011 upstream gene variant T/A;C snv 6
rs8176747
ABO
9 133255928 missense variant C/A;G snv 4.1E-06; 0.12 6
rs115810
TRIM38
0.925 0.120 6 25975655 intron variant G/A;C snv 5
rs12373142
SPPL2C ; MAPT-AS1
0.851 0.200 17 45846834 missense variant C/G;T snv 0.15 5
rs1256061
ESR2
14 64236875 intron variant G/A;T snv 5
rs13219787
H2AC17 ; H2BC17
6 27893892 upstream gene variant G/A;T snv 3.9E-02; 2.4E-04 5
rs1540276
H4C2
0.925 0.120 6 26028591 upstream gene variant T/A;G snv 5
rs199734 0.925 0.120 6 25940165 intergenic variant G/A;C snv 5
rs199737 0.925 0.120 6 25933310 upstream gene variant A/C;T snv 5
rs218264 4 54542708 intergenic variant A/G;T snv 5
rs2396083
LOC105375069 ; LOC107986598
0.882 0.160 6 43837071 intron variant G/A;C;T snv 5
rs2794719
LOC108783645 ; HFE
0.925 0.120 6 26088662 intron variant T/C;G snv 5
rs3218097
CCND3
6 41937537 intron variant G/A;T snv 5
rs33930165
HBB
0.882 0.120 11 5227003 missense variant C/G;T snv 9.2E-04; 4.4E-05 5
rs3752419
H4C2
0.882 0.160 6 26027205 synonymous variant G/A;C;T snv 0.41; 4.0E-06 5