Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11191580
NT5C2
0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 13
rs2246490 14 103517957 downstream gene variant G/T snv 0.67 1
rs11826048 11 103527569 intergenic variant C/T snv 9.6E-02 1
rs11111839
TTC41P
12 103916945 intron variant C/A snv 7.9E-02 1
rs4387287
STN1
10 103918139 5 prime UTR variant A/C snv 0.69 4
rs144588452
ABCA1
9 104784371 missense variant C/T snv 2.2E-04 1.5E-04 1
rs2066718
ABCA1
0.882 0.120 9 104826974 missense variant C/G;T snv 4.3E-04; 5.4E-02 7
rs2230806
ABCA1
0.689 0.280 9 104858586 missense variant C/T snv 0.32 0.39 24
rs145158522
SORCS3
10 104870101 intron variant C/A;G;T snv 1
rs35783704
ZFPM2
8 104954030 intron variant G/A snv 7.2E-02 2
rs56388530
NPNT
4 105989801 intron variant C/A;T snv 2
rs17477177 1.000 0.080 7 106771412 upstream gene variant T/C snv 0.17 4
rs373644334
PIK3CG
7 106867748 missense variant G/A;C;T snv 4.0E-06; 4.0E-06; 4.0E-06 1
rs4754196
LOC105369477
11 107226051 intergenic variant A/G snv 0.39 1
rs880315
CASZ1
0.925 0.120 1 10736809 intron variant T/C snv 0.32 9
rs12212067
FOXO3
0.716 0.320 6 108659993 intron variant T/G snv 0.14 20
rs3087456
CIITA ; LOC105371080
0.742 0.480 16 10877045 intron variant G/A snv 0.53 14
rs4774
CIITA
0.807 0.240 16 10906991 missense variant G/C snv 0.30 0.28 7
rs12740374
CELSR2
0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 16
rs1887320 20 10985350 intron variant G/A snv 0.46 6
rs9634314
TCHP ; GIT2
12 109968581 intron variant G/A snv 0.20 1
rs10816914
PALM2AKAP2
9 109998608 intron variant G/A snv 0.40 1
rs675605
COL4A1
13 110221209 intron variant G/A;C snv 1
rs2855469
MXI1
10 110281821 intron variant T/C snv 0.43 1
rs1285539239
COL4A2 ; COL4A2-AS2
13 110462280 missense variant G/A snv 4.0E-06 1