Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10455152 1.000 0.080 6 85308630 intergenic variant A/C snv 0.29 1
rs1081105
APOE
1.000 0.080 19 44909698 non coding transcript exon variant A/C snv 3.0E-02 1
rs10997691
CTNNA3
1.000 0.080 10 67521827 intron variant A/C snv 0.16 0.13 1
rs11603136 1.000 0.080 11 86163280 regulatory region variant A/C snv 0.41 1
rs1167428194
APOE
1.000 0.080 19 44908634 missense variant A/C snv 1
rs11773349
LOC105375328
1.000 0.080 7 64946786 upstream gene variant A/C snv 0.12 1
rs117983694
CCDC89
1.000 0.080 11 85685837 missense variant A/C snv 5.4E-03 6.0E-03 1
rs1408077
CR1
1.000 0.080 1 207630796 intron variant A/C snv 0.84 1
rs1408585874
CAMK1 ; OGG1
1.000 0.080 3 9757233 missense variant A/C snv 4.0E-06 1
rs17014873
BIN1
1.000 0.080 2 127072643 intron variant A/C snv 0.11 1
rs17172199
HECW1
1.000 0.080 7 43337677 intron variant A/C snv 5.2E-02 1
rs183562580
OTOF
1.000 0.080 2 26471784 intron variant A/C snv 1
rs192093332 1.000 0.080 8 83267319 intergenic variant A/C snv 1
rs2015475
MS4A4E ; MS4A4A
1.000 0.080 11 60231490 intron variant A/C snv 0.32 1
rs2274705
ESR2
1.000 0.080 14 64249911 intron variant A/C snv 0.18 1
rs326946
ARHGAP20
1.000 0.080 11 110628530 intron variant A/C snv 0.26 1
rs4663105
LOC105373605
1.000 0.080 2 127133851 intergenic variant A/C snv 0.47 1
rs4844610
CR1
1.000 0.080 1 207629207 intron variant A/C snv 0.87 1
rs714948
LOC107985305 ; CEACAM19 ; PVR
1.000 0.080 19 44662645 3 prime UTR variant A/C snv 0.92 1
rs73052335
APOC1
1.000 0.080 19 44916825 intron variant A/C snv 8.6E-02 1
rs75617873
PARVB
1.000 0.080 22 44130225 intron variant A/C snv 2.3E-02 1
rs7575209
LOC105373605
1.000 0.080 2 127126547 intergenic variant A/C snv 0.22 1
rs777203282
ECE2 ; EEF1AKMT4-ECE2
1.000 0.080 3 184277413 missense variant A/C snv 1
rs7933202 1.000 0.080 11 60169453 downstream gene variant A/C snv 0.28 1
rs79781504 1.000 0.080 8 83837822 intergenic variant A/C snv 6.2E-03 1