Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1458103 11 81336231 intron variant A/C snv 0.25 1
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
rs11059336 12 127745489 regulatory region variant T/C snv 0.14 1
rs1051730
CHRNA3
0.641 0.600 15 78601997 synonymous variant G/A snv 0.27 0.26 11
rs16969968
CHRNA5
0.653 0.360 15 78590583 missense variant G/A snv 0.26 0.24 4
rs11855560
RAD51
15 40732105 3 prime UTR variant T/C snv 0.49 1
rs5882
CETP
0.649 0.400 16 56982180 missense variant G/A;C snv 0.62 3
rs34516333
ZFHX3
16 73114768 intron variant G/T snv 0.17 1
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
rs12454712
BCL2
0.925 0.120 18 63178651 intron variant T/A;C snv 7
rs11669576
LDLR ; MIR6886
0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 1
rs3918242
MMP9
0.602 0.680 20 46007337 upstream gene variant C/T snv 0.14 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
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