Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11549465
HIF1A-AS3 ; HIF1A
0.597 0.680 14 61740839 missense variant C/T snv 8.8E-02 7.7E-02 55
rs11574
ID3
1.000 0.040 1 23559007 missense variant T/A;C snv 0.80 2
rs11575937
LMNA
0.653 0.480 1 156136985 missense variant G/A;T snv 29
rs11615
ERCC1
0.572 0.640 19 45420395 synonymous variant A/G snv 0.50 0.55 62
rs11622435
LOC101928462
0.827 0.120 14 81151652 intron variant G/A snv 4.7E-02 7
rs11672433
ANGPTL4
0.925 0.120 19 8373832 synonymous variant G/A;C snv 0.10; 4.0E-06 3
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1169305
HNF1A
1.000 0.040 12 120999579 missense variant A/G snv 1.00 0.99 2
rs11712619
KALRN
0.882 0.160 3 124300955 intron variant C/A;T snv 0.26 5
rs1174670182
GCK
0.925 0.080 7 44145616 synonymous variant A/T snv 7.0E-06 3
rs11771443
NOS3
0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs118081497
EEA1
1.000 0.040 12 92782070 missense variant A/T snv 1.1E-02 3.3E-03 2
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs11868035
RAI1 ; SREBF1
0.763 0.200 17 17811787 splice region variant G/A snv 0.45 0.33 14
rs1187274
NTRK2
1.000 0.040 9 84804874 intron variant C/G snv 0.55 2
rs1188383936
F2
0.524 0.760 11 46725976 missense variant C/T snv 8.0E-06 102
rs11915160
SOX2 ; SOX2-OT
0.851 0.200 3 181713783 3 prime UTR variant C/A snv 0.11 5
rs11920090
SLC2A2
1.000 0.040 3 170999732 intron variant T/A snv 0.20 5
rs12026
PON2
0.827 0.240 7 95411704 missense variant G/C snv 0.27 0.27 6
rs1205
CRP
0.602 0.680 1 159712443 3 prime UTR variant C/T snv 0.30 46
rs1206634 1.000 0.040 X 96302380 intron variant T/A;G snv 2
rs12104705
KCNH7
0.882 0.120 2 162435107 intron variant C/T snv 0.15 4
rs12107
MYH9
1.000 0.040 22 36281936 3 prime UTR variant G/A;T snv 3
rs12144939
CFH
0.925 0.080 1 196729815 intron variant G/A;T snv 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614