Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1800764 0.790 0.320 17 63473168 upstream gene variant C/G;T snv 10
rs1187120 0.925 0.040 6 34182850 intergenic variant T/C snv 0.99 3
rs9877502 0.925 0.080 3 190951729 intergenic variant G/A snv 0.40 3
rs1157659 1.000 0.040 11 27736075 intron variant A/G snv 0.37 2
rs1557372 1.000 0.040 21 41460614 downstream gene variant C/T snv 0.40 2
rs16885997 8 114496877 intergenic variant G/T snv 3.5E-02 1
rs7700443 5 85876294 intergenic variant T/G snv 0.57 1
rs3764650
ABCA7
0.790 0.200 19 1046521 intron variant T/G snv 0.14 9
rs16947151
ABI3
0.882 0.080 17 49213276 intron variant A/G snv 0.12 4
rs4291
ACE
0.724 0.400 17 63476833 upstream gene variant T/A;C snv 20
rs761715536
ADRA2A
1.000 0.040 10 111079092 stop gained G/A;T snv 6.4E-06; 1.3E-05 3
rs5978930
ANOS1
0.882 0.080 X 8642266 intron variant T/C;G snv 4
rs10512015
ANXA1
9 73166330 intron variant T/C snv 9.9E-02 1
rs4420638
APOC1
0.708 0.520 19 44919689 downstream gene variant A/G snv 0.18 43
rs429358
APOE
0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs769449
APOE
0.882 0.120 19 44906745 non coding transcript exon variant G/A snv 8.4E-02 11
rs267606663
APOE
0.925 0.080 19 44909021 missense variant G/A;C snv 7.3E-06 3
rs1231783932
APP
0.763 0.120 21 26051171 missense variant T/A;C snv 1.2E-05 11
rs63750847
APP
0.790 0.120 21 25897620 missense variant C/T snv 4.5E-04 3.0E-04 8
rs1396086494
APP
0.851 0.080 21 26051069 missense variant G/A snv 4.0E-06 6
rs193922916
APP
0.827 0.080 21 25897619 missense variant G/A;C snv 6
rs9951307
AQP4-AS1
0.882 0.120 18 26850565 intron variant G/A snv 0.65 5
rs3763040
AQP4 ; AQP4-AS1
0.925 0.080 18 26864410 intron variant G/A;T snv 3
rs3763043
AQP4 ; AQP4-AS1
0.925 0.080 18 26855854 3 prime UTR variant C/T snv 0.30 3
rs3875089
AQP4 ; AQP4-AS1
0.925 0.080 18 26865469 intron variant T/C snv 0.19 3