Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1012381950
POLB
1.000 0.080 8 42353758 intron variant T/C snv 1
rs10197851
HPCAL1
1.000 0.080 2 10345283 intron variant A/G snv 0.52 1
rs1035071612
MIR6886 ; LDLR
0.763 0.240 19 11113361 missense variant C/A;T snv 4.0E-06 9
rs10410544
SIRT2
0.827 0.120 19 38894892 intron variant T/C snv 0.68 0.67 6
rs10410711
ZNF566
1.000 0.080 19 36449796 synonymous variant A/G snv 3.3E-02 3.5E-02 1
rs10421862
ZNF566
1.000 0.080 19 36474174 intron variant G/T snv 0.10 1
rs10498633
SLC24A4
0.925 0.080 14 92460608 intron variant G/T snv 0.19 2
rs1050283
OLR1
0.882 0.160 12 10159690 3 prime UTR variant G/A snv 0.40 4
rs1050286
OLR1
0.882 0.160 12 10158964 3 prime UTR variant T/C snv 0.40 3
rs1051338
LIPA
0.807 0.120 10 89247603 missense variant T/G snv 0.32 0.26 7
rs10524523
TOMM40
0.807 0.200 19 44899792 intron variant TTTTTTTTTTTTTTTTTTTTTTT/-;T;TT;TTT;TTTT;TTTTT;TTTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT delins 7
rs1059507
LPL
1.000 0.080 8 19966452 3 prime UTR variant C/T snv 0.15 4
rs1060743
BIN1
0.925 0.080 2 127068957 synonymous variant A/G snv 0.34 0.29 2
rs1061170
CFH
0.561 0.720 1 196690107 missense variant C/T snv 0.68 0.64 72
rs10824310
PRKG1-AS1 ; PRKG1
1.000 0.080 10 52268704 intron variant C/T snv 4.7E-02 1
rs10845990
SLC2A14
0.925 0.080 12 7818125 intron variant T/A;G snv 2
rs10997477
LOC101928961 ; CTNNA3 ; LRRTM3
1.000 0.080 10 67000961 intron variant C/T snv 0.31 1
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1117750
DGKB
1.000 0.080 7 14848793 intron variant C/T snv 0.10 1
rs11190302 1.000 0.080 10 99873158 downstream gene variant C/T snv 0.37 1
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
rs1131445
IL16 ; STARD5
0.724 0.440 15 81309441 3 prime UTR variant T/A;C snv 16
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs1155002
CYP2J2
1.000 0.080 1 59908103 intron variant T/C snv 0.66 2