Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4692589
MFAP3L
4 170014094 intron variant A/G snv 0.44 1
rs4951043
SOX13
1 204105737 intron variant C/T snv 0.51 1
rs6030245
PTPRT
20 42441919 intron variant T/C snv 0.30 1
rs63750579
APP
0.742 0.280 21 25891856 missense variant C/G;T snv 1
rs6462203
SDK1
7 3636370 intron variant C/A;T snv 1
rs72711240 4 134774652 intron variant C/T snv 2.2E-02 1
rs79928194
GIGYF2
2 232784580 intron variant T/C snv 0.14 1
rs9875578 3 13752941 intergenic variant G/A;C snv 1
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 5
rs202085145
SUOX
1.000 0.080 12 56002720 missense variant G/T snv 1.0E-03 5.6E-04 6
rs1800562
LOC108783645 ; HFE
0.435 0.880 6 26092913 missense variant G/A snv 3.3E-02 3.8E-02 34
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
rs6265
BDNF ; BDNF-AS
0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 8
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs324981
NPSR1-AS1 ; NPSR1
0.724 0.320 7 34778501 missense variant A/T snv 0.44 0.47 1
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3