Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs5786996
IDE
1.000 0.080 10 92452778 3 prime UTR variant -/G delins 3.4E-02 1
rs1925608
LRRTM3 ; CTNNA3 ; LOC101928961
1.000 0.080 10 66990654 intron variant A/C snv 0.49 1
rs4417206
ALDH18A1
1.000 0.080 10 95636713 intron variant A/C snv 0.28 1
rs12344615
UBQLN1
0.851 0.080 9 83666280 intron variant A/C;G snv 4
rs4147929
ABCA7
0.882 0.120 19 1063444 intron variant A/C;G snv 3
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs1695
GSTP1
0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1137101
LEPR
0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 77
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs768623239
GSTM1 ; GSTM2
0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs334558
LOC107986119 ; GSK3B
0.701 0.320 3 120094435 upstream gene variant A/G snv 0.51 20
rs2274567
CR1
0.776 0.400 1 207580276 missense variant A/G snv 0.25 0.21 10
rs6859
NECTIN2
0.827 0.120 19 44878777 3 prime UTR variant A/G snv 0.58 10
rs744373 0.851 0.160 2 127137039 downstream gene variant A/G snv 0.35 8
rs2986017
CALHM1
0.851 0.120 10 103458495 missense variant A/G snv 0.79 0.80 6
rs3818361
CR1
0.851 0.080 1 207611623 intron variant A/G snv 0.74 6
rs754203
CYP46A1
0.807 0.200 14 99691630 non coding transcript exon variant A/G snv 0.27 6
rs12570088 0.851 0.160 10 58178575 intergenic variant A/G snv 4.1E-02 4
rs2234256
TREML1 ; LOC105375056 ; TREM2
0.882 0.120 6 41158917 missense variant A/G snv 1.8E-02 4.0E-02 3
rs4646953
IDE
0.882 0.160 10 92574198 upstream gene variant A/G snv 0.17 3
rs1060743
BIN1
0.925 0.080 2 127068957 synonymous variant A/G snv 0.34 0.29 2
rs11218304
LOC105369535 ; SORL1
0.925 0.080 11 121478402 intron variant A/G snv 0.30 2
rs115865530
PSEN1
0.925 0.080 14 73206449 missense variant A/G snv 1.4E-04 4.2E-05 2
rs1369330655
CTSD
0.925 0.080 11 1761421 missense variant A/G snv 7.0E-06 2