Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs1006737
CACNA1C
0.695 0.120 12 2236129 intron variant G/A snv 0.36 7
rs202085145
SUOX
1.000 0.080 12 56002720 missense variant G/T snv 1.0E-03 5.6E-04 6
rs3093662
TNF
0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 6
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 5
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 5
rs5742905
CBS
0.701 0.360 21 43063074 missense variant A/G snv 4
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs6855911
SLC2A9
0.851 0.200 4 9934286 intron variant A/G snv 0.33 4
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs63750264
APP
0.716 0.360 21 25891784 missense variant C/A;G;T snv 2
rs1709393
LINC02085
1.000 0.080 3 101980310 intron variant C/T snv 0.55 2
rs7528604
PDE4B
0.925 0.040 1 65941669 intron variant G/A snv 0.42 2
rs104893877
SNCA
0.614 0.360 4 89828149 missense variant C/T snv 2
rs11059336 12 127745489 regulatory region variant T/C snv 0.14 1
rs113209956 9 25211195 intergenic variant C/T snv 5.4E-02 1
rs1192553 1 17967858 intergenic variant G/A snv 0.70 1
rs1458103 11 81336231 intron variant A/C snv 0.25 1
rs72711240 4 134774652 intron variant C/T snv 2.2E-02 1
rs9875578 3 13752941 intergenic variant G/A;C snv 1
rs2451828
ADCY2
5 7448683 intron variant C/T snv 2.7E-02 1
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 1