Disease: Diabetes
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7212
TXNIP
0.851 0.120 1 145992816 3 prime UTR variant G/C snv 0.16 5
rs10757283 0.827 0.120 9 22134173 intergenic variant C/A;T snv 0.45 6
rs7211
TXNIP
0.827 0.200 1 145993449 3 prime UTR variant G/A;C;T snv 6
rs17366743
ADIPOQ-AS1 ; ADIPOQ
0.807 0.280 3 186854300 missense variant T/C snv 2.2E-02 2.1E-02 7
rs9267551
CLIC1 ; DDAH2
0.807 0.160 6 31730180 5 prime UTR variant C/G;T snv 7
rs5082
APOA2
0.807 0.160 1 161223893 upstream gene variant G/A snv 0.68 8
rs775381348
PSMA6
0.807 0.160 14 35308023 missense variant G/T snv 8
rs3732581
PARL
0.790 0.120 3 183840614 missense variant C/G;T snv 0.46; 1.2E-05 9
rs4717806
LOC105375350 ; STX1A ; BUD23
0.776 0.200 7 73702147 intron variant T/A;C snv 9
rs6850
LOC105375259 ; PPIA
0.790 0.160 7 44796715 5 prime UTR variant A/G;T snv 0.26; 4.0E-06 9
rs10911021
LOC105371642 ; LINC01344
0.807 0.160 1 182112825 intron variant C/T snv 0.36 11
rs1320702652
MFAP1
0.752 0.160 15 43824536 missense variant G/A snv 4.0E-06 11
rs185847354
ADIPOQ ; ADIPOQ-AS1
0.763 0.160 3 186854460 missense variant T/C snv 3.1E-04 7.0E-05 11
rs201058276
F7
0.776 0.240 13 113118731 missense variant G/A;C snv 4.8E-05; 4.0E-06 11
rs17568
TNFRSF4
0.752 0.320 1 1212042 synonymous variant C/T snv 0.37 0.31 12
rs20455
KIF6 ; LOC107986594
0.763 0.160 6 39357302 missense variant A/G snv 0.41 0.49 12
rs1129844
CCL11
0.752 0.320 17 34285875 missense variant G/A;C;T snv 0.16; 1.2E-05 13
rs1131498
C1orf112 ; SELL
0.732 0.360 1 169707345 missense variant A/G snv 0.21 0.22 13
rs9282541
ABCA1
0.790 0.160 9 104858554 missense variant G/A snv 1.3E-02 4.4E-03 13
rs1063856
VWF
0.763 0.400 12 6044368 missense variant T/C;G snv 0.31 14
rs11066001
BRAP
0.763 0.360 12 111681367 intron variant T/C snv 5.8E-03 15
rs184003
AGER
0.724 0.400 6 32182519 intron variant C/A snv 0.12 0.12 15
rs1800588
ALDH1A2 ; LIPC
0.790 0.200 15 58431476 intron variant C/G;T snv 0.30 16
rs2016520
PPARD
0.752 0.320 6 35411001 5 prime UTR variant C/T snv 0.78 16
rs2295490
TRIB3
0.724 0.320 20 388261 missense variant A/G;T snv 0.18; 4.0E-06 16