Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7671266
SLC2A9
0.925 0.120 4 10054752 intron variant T/C snv 0.73 4
rs9291683 0.925 0.120 4 10322536 intergenic variant G/A;C;T snv 4
rs4698036 0.925 0.120 4 10329670 intergenic variant T/G snv 0.21 4
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs660240
CELSR2
1 109275216 3 prime UTR variant T/C snv 0.75 6
rs646776
CELSR2
0.752 0.240 1 109275908 downstream gene variant C/T snv 0.74 25
rs599839
PSRC1
0.724 0.360 1 109279544 downstream gene variant G/A;C snv 27
rs6511720
LDLR
0.790 0.120 19 11091630 intron variant G/T snv 0.12 15
rs964184
ZPR1
0.716 0.440 11 116778201 3 prime UTR variant G/C snv 0.82 47
rs6589566
ZPR1
0.882 0.080 11 116781707 intron variant G/A;C;T snv 10
rs2075290
ZPR1
0.882 0.160 11 116782580 intron variant C/G;T snv 10
rs2266788
APOA5 ; ZPR1
0.763 0.440 11 116789970 3 prime UTR variant G/A snv 0.93 19
rs508487
TAGLN ; PCSK7
11 117204850 3 prime UTR variant C/T snv 5.2E-02 4
rs1047964
BACE1 ; RNF214
11 117286177 3 prime UTR variant G/A;C;T snv 3
rs2650000
HNF1A-AS1
0.851 0.200 12 120951159 intron variant A/C snv 0.70 10
rs1169288
HNF1A-AS1 ; HNF1A
0.776 0.160 12 120978847 missense variant A/C;T snv 0.35 21
rs1183910
HNF1A
1.000 0.080 12 120983004 intron variant G/A snv 0.28 5
rs7310409
HNF1A
0.925 0.160 12 120987058 intron variant A/C;G;T snv 7
rs2259816
HNF1A
0.827 0.280 12 120997784 synonymous variant G/A;T snv 6.7E-06; 0.40 8
rs1169310
C12orf43 ; HNF1A
12 121001630 3 prime UTR variant G/A snv 0.31 3
rs1169313
C12orf43
12 121004867 intron variant T/A;C snv 6
rs3213545
OASL
12 121033534 synonymous variant G/A snv 0.32 0.26 3
rs2009865 11 127909930 intergenic variant T/C snv 1
rs687621
ABO
0.851 0.240 9 133261662 intron variant G/A;C snv 18