Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800797
IL6 ; IL6-AS1 ; STEAP1B
0.605 0.800 7 22726602 non coding transcript exon variant A/G snv 0.72 43
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs1800625
AGER ; PBX2
0.641 0.680 6 32184665 upstream gene variant A/G snv 0.15 39
rs2670660
NLRP1
0.708 0.400 17 5615686 intron variant A/G snv 0.41 15
rs1926447
CPB2 ; CPB2-AS1
0.807 0.440 13 46055809 missense variant A/G snv 0.74 0.77 11
rs2241767
ADIPOQ-AS1 ; ADIPOQ
0.763 0.440 3 186853407 intron variant A/G snv 0.10 10
rs5030717
TLR4
0.807 0.240 9 117711556 intron variant A/G snv 0.13 9
rs4293393
UMOD
0.827 0.200 16 20353266 intron variant A/G snv 0.20 8
rs3818292
SIRT1
0.827 0.280 10 67907144 intron variant A/G snv 7.1E-02 5
rs7211818
RPTOR
0.827 0.200 17 80715103 intron variant A/G snv 0.23 5
rs10770125
INS-IGF2 ; IGF2 ; IGF2-AS
0.882 0.200 11 2147784 missense variant A/G snv 0.49 0.40 4
rs1400094618
MOK
0.882 0.240 14 102229508 missense variant A/G snv 3
rs2305619
VEPH1 ; PTX3
0.882 0.240 3 157437072 intron variant A/G snv 0.55 0.50 3
rs955333 0.882 0.240 6 154626274 intergenic variant A/G snv 0.13 3
rs10255208 0.925 0.160 7 36819038 non coding transcript exon variant A/G snv 0.46 2
rs2796498
PRKAA2
0.925 0.160 1 56678313 intron variant A/G snv 0.47 2
rs9674559
RPTOR
0.925 0.160 17 80741808 intron variant A/G snv 0.22 2
rs10047560
PDE3A
1.000 0.120 12 20452282 intron variant A/G snv 0.86 1
rs10868025
FRMD3
1.000 0.120 9 83549261 intergenic variant A/G snv 0.30 1
rs11645214
SF3B3
1.000 0.120 16 70575084 3 prime UTR variant A/G snv 0.39 1
rs1249910 1.000 0.120 3 112672327 intergenic variant A/G snv 0.58 1
rs1253192 1.000 0.120 14 59376688 intergenic variant A/G snv 0.92 1
rs140407862
WFS1
1.000 0.120 4 6301015 missense variant A/G snv 4.4E-05 1.0E-04 1
rs17297207
NFAT5
1.000 0.120 16 69609450 intron variant A/G snv 5.9E-02 1
rs6499323
IL34
1.000 0.120 16 70590580 intron variant A/G snv 0.23 1