Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2069840
IL6 ; IL6-AS1
0.742 0.360 7 22728953 intron variant C/G snv 0.27 13
rs1275805226
AGT
0.776 0.240 1 230706148 frameshift variant G/- del 7.0E-06 12
rs1532624
CETP
0.851 0.160 16 56971567 intron variant C/A snv 0.34 12
rs281432
ICAM1
0.851 0.280 19 10279982 intron variant C/G snv 0.52 12
rs7756992
CDKAL1
0.827 0.240 6 20679478 intron variant A/G;T snv 12
rs17300539
ADIPOQ
0.752 0.320 3 186841671 upstream gene variant G/A snv 5.3E-02 11
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs2082940
ADIPOQ-AS1 ; ADIPOQ
0.763 0.480 3 186856375 3 prime UTR variant T/A;C snv 10
rs2241767
ADIPOQ-AS1 ; ADIPOQ
0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs290487
TCF7L2
0.776 0.280 10 113149972 intron variant C/T snv 0.16 10
rs3865188 0.790 0.320 16 82617112 intergenic variant A/G;T snv 10
rs3918188
NOS3
0.776 0.280 7 151005693 intron variant C/A;T snv 10
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs7679
PCIF1
0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 9
rs11771443
NOS3
0.790 0.360 7 150990599 upstream gene variant C/T snv 0.16 8
rs3917887
CCL2
0.776 0.240 17 34255979 non coding transcript exon variant AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC delins 0.33 8
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs1332629192
ALB
0.851 0.200 4 73404374 missense variant C/T snv 7
rs1800783
NOS3
0.827 0.280 7 150992309 intron variant A/C;G;T snv 7
rs1063537
ADIPOQ-AS1 ; ADIPOQ
0.807 0.320 3 186856286 3 prime UTR variant C/T snv 9.6E-02 6
rs11646213 0.827 0.320 16 82609046 intergenic variant A/T snv 0.47 6
rs2237897
KCNQ1
0.882 0.200 11 2837316 intron variant C/T snv 8.1E-02 6
rs2268388
ACACB
0.851 0.200 12 109205840 intron variant G/A snv 0.14 6
rs6495446
MTHFS ; ST20-MTHFS
0.851 0.200 15 79862640 intron variant C/T snv 0.31 6
rs759853
AKR1B1
0.827 0.320 7 134459206 non coding transcript exon variant G/A snv 0.33 6