Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9472817
LOC101926934 ; SLC25A27
0.882 0.080 6 46673255 intron variant C/G;T snv 3
rs10498633
SLC24A4
0.925 0.080 14 92460608 intron variant G/T snv 0.19 2
rs1060743
BIN1
0.925 0.080 2 127068957 synonymous variant A/G snv 0.34 0.29 2
rs10845990
SLC2A14
0.925 0.080 12 7818125 intron variant T/A;G snv 2
rs11218304
LOC105369535 ; SORL1
0.925 0.080 11 121478402 intron variant A/G snv 0.30 2
rs11218343
SORL1
0.925 0.080 11 121564878 intron variant T/A;C snv 2
rs1155002
CYP2J2
1.000 0.080 1 59908103 intron variant T/C snv 0.66 2
rs115865530
PSEN1
0.925 0.080 14 73206449 missense variant A/G snv 1.4E-04 4.2E-05 2
rs11610206
LOC105369746
0.925 0.080 12 47245743 intron variant T/C snv 9.7E-02 2
rs11771145
EPHA1-AS1
0.925 0.080 7 143413669 intron variant G/A snv 0.42 2
rs1369330655
CTSD
0.925 0.080 11 1761421 missense variant A/G snv 7.0E-06 2
rs137875858
UNC5C
0.925 0.080 4 95170280 missense variant G/A snv 2.9E-04 2.6E-04 2
rs1385600
USP35 ; GAB2
0.925 0.080 11 78225120 synonymous variant A/G snv 0.25 0.27 2
rs145999145
PLD3
0.925 0.080 19 40371688 missense variant G/A snv 3.1E-03 3.6E-03 2
rs1476679
ZCWPW1
0.925 0.080 7 100406823 intron variant C/A;T snv 4.0E-06; 0.74 2
rs1532278
CLU
0.925 0.080 8 27608798 non coding transcript exon variant T/C snv 0.68 2
rs1562990
MS4A4A
0.925 0.080 11 60255614 intron variant C/A;T snv 2
rs165932
PSEN1
0.925 0.080 14 73198145 intron variant G/A;T snv 0.61 2
rs17277986
SORCS1
0.925 0.080 10 106998968 intron variant C/T snv 0.22 2
rs190982
MEF2C-AS1
0.925 0.080 5 88927603 intron variant G/A snv 0.72 2
rs1992269 0.925 0.080 18 1872316 intron variant C/T snv 0.24 2
rs200529365
PLD3 ; MIR6796
0.925 0.080 19 40369967 missense variant C/G;T snv 2.3E-04; 1.2E-05 2
rs200620364
APP
0.925 0.080 21 26021849 missense variant C/T snv 2
rs2373115
GAB2
0.925 0.080 11 78380104 intron variant C/A snv 0.24 2
rs2651206
TTBK1
0.925 0.080 6 43245739 intron variant C/T snv 0.47 2