Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217777010
APOA1-AS ; APOA1
1.000 0.040 11 116836182 missense variant C/T snv 4.0E-06 1
rs7982
CLU
1.000 0.040 8 27604964 missense variant A/C;G snv 0.64 0.60 1
rs1309900188
GSN
1.000 0.040 9 121312342 missense variant A/G;T snv 4.0E-06; 4.0E-06 1
rs535229743
GSN
1.000 0.040 9 121327419 missense variant G/A;C snv 1
rs1454603223
LYZ
1.000 0.040 12 69353160 missense variant T/C snv 4.0E-06 7.0E-06 1
rs1294297409
TTR
1.000 0.040 18 31592996 missense variant C/A snv 8.0E-06 1
rs62093482
TTR
1.000 0.040 18 31598936 3 prime UTR variant C/T snv 1.8E-02 1
rs200538373
ABCA7
0.925 0.120 19 1061893 splice region variant G/A;C snv 2.5E-03 2
rs10097505
ARC
0.925 0.120 8 142612823 3 prime UTR variant G/A snv 0.47 2
rs371557337
DCTN4
1.000 0.040 5 150733475 start lost T/C;G snv 7.0E-06 2
rs1473654052
DOCK11
0.925 0.080 X 118542729 missense variant A/C snv 9.5E-06 2
rs1335856860
FAP
0.925 0.120 2 162183437 missense variant T/C snv 7.0E-06 2
rs1264519280
KHDRBS1
1.000 0.040 1 32014083 missense variant G/A snv 2
rs1440063914
KIDINS220
0.925 0.080 2 8779781 missense variant T/C snv 2
rs13031703
LOC105373605
0.925 0.120 2 127129099 intergenic variant C/T snv 0.11 2
rs767006697
MEFV
0.925 0.080 16 3254658 frameshift variant C/- delins 2
rs933476040
TTR
0.925 0.120 18 31595130 missense variant G/A snv 2
rs766474822
VEGFA
0.925 0.080 6 43770990 missense variant G/A snv 1.4E-05 2.1E-05 2
rs201564694
APCS
0.882 0.120 1 159588626 missense variant T/C snv 3
rs529782627
APP
0.882 0.120 21 26112051 missense variant C/A snv 4.0E-06 7.0E-06 3
rs763852444
APP
0.882 0.120 21 26112127 missense variant G/C snv 4.0E-06 3
rs371792178
DPYD
0.925 0.040 1 97699507 missense variant G/A;C snv 3.6E-05; 1.2E-05 3
rs121913549
LYZ
0.882 0.200 12 69350194 missense variant T/A snv 3
rs80356710
PRNP
0.925 0.040 20 4699655 stop gained T/G snv 3
rs121918077
TTR
0.882 0.120 18 31592992 missense variant G/C snv 3