Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs140407862
WFS1
1.000 0.120 4 6301015 missense variant A/G snv 4.4E-05 1.0E-04 1
rs1411766
LOC101927627
0.882 0.160 13 109599813 intron variant G/A;T snv 3
rs1416580204
MOK
0.608 0.720 14 102250837 missense variant C/T snv 4.0E-06 7.0E-06 49
rs14259
PSMD9
0.724 0.360 12 121915890 missense variant A/C;G snv 4.0E-06; 0.32 19
rs143101792
CRP
0.851 0.320 1 159714026 stop gained G/C snv 8.8E-05 1.3E-04 5
rs1476046
EDN1
1.000 0.120 6 12292988 intron variant G/A snv 0.22 1
rs1501299
ADIPOQ ; ADIPOQ-AS1
0.597 0.720 3 186853334 intron variant G/C;T snv 52
rs1531343
RPSAP52
0.925 0.160 12 65781114 intron variant G/C;T snv 2
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs1549758
NOS3
0.807 0.360 7 150998638 synonymous variant T/C snv 0.76 0.76 7
rs1567438
LPAL2
0.925 0.200 6 160458599 intron variant T/C snv 0.25 3
rs16139
NPY ; LOC107986777
0.658 0.560 7 24285260 missense variant T/A;C snv 4.0E-06; 3.0E-02 36
rs16835198 0.882 0.200 1 32861080 downstream gene variant G/T snv 0.29 3
rs16928973
TRAF6
0.925 0.160 11 36492695 intron variant C/T snv 1.2E-02 2
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs16996381 1.000 0.120 22 36115231 intergenic variant G/A snv 0.31 1
rs17297207
NFAT5
1.000 0.120 16 69609450 intron variant A/G snv 5.9E-02 1
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs17300593 0.925 0.160 1 58637536 intergenic variant C/G snv 2
rs17446614
FOXO1
0.851 0.240 13 40565740 intron variant G/A snv 0.16 5
rs17471
LOC107986119
1.000 0.120 3 120098826 non coding transcript exon variant A/T snv 6.3E-02 1
rs17576
MMP9
0.557 0.760 20 46011586 missense variant A/G snv 0.39 0.36 73
rs17592236
FOXO1
0.925 0.200 13 40557795 3 prime UTR variant C/T snv 3.7E-02 2
rs17809399
LARGE1
1.000 0.120 22 33861145 intron variant G/A snv 0.21 1