Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1709393
LINC02085
1.000 0.080 3 101980310 intron variant C/T snv 0.55 2
rs11669576
LDLR ; MIR6886
0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 1
rs1143634
IL1B
0.597 0.680 2 112832813 synonymous variant G/A snv 0.19 0.19 1
rs10893268
OR8A1
11 124568716 intron variant C/T snv 0.40 1
rs11059336 12 127745489 regulatory region variant T/C snv 0.14 1
rs72711240 4 134774652 intron variant C/T snv 2.2E-02 1
rs9875578 3 13752941 intergenic variant G/A;C snv 1
rs4692589
MFAP3L
4 170014094 intron variant A/G snv 0.44 1
rs1192553 1 17967858 intergenic variant G/A snv 0.70 1
rs4951043
SOX13
1 204105737 intron variant C/T snv 0.51 1
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs79928194
GIGYF2
2 232784580 intron variant T/C snv 0.14 1
rs113209956 9 25211195 intergenic variant C/T snv 5.4E-02 1
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 2
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 1
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs1799964
LTA ; LOC100287329 ; TNF
0.608 0.760 6 31574531 upstream gene variant T/C snv 0.19 1
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 1
rs1360780
FKBP5 ; LOC112267956
0.708 0.320 6 35639794 intron variant T/A;C snv 1
rs6462203
SDK1
7 3636370 intron variant C/A;T snv 1
rs11855560
RAD51
15 40732105 3 prime UTR variant T/C snv 0.49 1
rs6030245
PTPRT
20 42441919 intron variant T/C snv 0.30 1
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 4