Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1998122
DTD1
1.000 0.040 20 18727895 intron variant G/A snv 0.31 1
rs2695121
NR1H2
0.716 0.280 19 50377484 5 prime UTR variant T/C snv 0.70 16
rs11669576
LDLR ; MIR6886
0.851 0.160 19 11111624 missense variant G/A snv 4.3E-02 8.4E-02 6
rs112591851
FPR1
1.000 0.040 19 51749131 intron variant C/T snv 2.1E-02 1
rs77432625
PALM
1.000 0.040 19 727401 intron variant C/G snv 3.8E-02 1
rs1555743003
ASXL3
0.701 0.520 18 33740444 splice donor variant G/A snv 58
rs1555640521
LAMA1
0.790 0.320 18 6942110 frameshift variant A/- delins 15
rs10871777 0.925 0.120 18 60184530 intergenic variant A/G snv 0.24 6
rs62081501 0.925 0.080 18 37627749 intron variant G/A snv 6.2E-02 4
rs11663050 1.000 0.040 18 37621190 intron variant T/G snv 0.51 1
rs12957516
LOC107985118
1.000 0.040 18 37635554 intron variant C/T snv 0.54 1
rs1427041 1.000 0.040 18 37628357 intron variant A/G;T snv 1
rs1539844
CELF4
1.000 0.040 18 37540169 intron variant G/A snv 0.12 1
rs3897644 1.000 0.040 18 60061837 intergenic variant C/T snv 0.48 1
rs4799723
LOC107985157
1.000 0.040 18 33787086 intergenic variant T/A;G snv 1
rs62081537 1.000 0.040 18 37668124 intron variant T/C snv 0.16 1
rs62096058 1.000 0.040 18 60229853 intergenic variant G/A snv 0.34 1
rs72893199 1.000 0.040 18 37602745 intron variant T/C snv 0.18 1
rs9966951 1.000 0.040 18 60108063 intergenic variant G/A snv 0.34 1
rs25531
SLC6A4 ; LOC105371720
0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs63751273
MAPT
0.645 0.280 17 46010389 missense variant C/T snv 42
rs63750424
MAPT
0.677 0.240 17 46024061 missense variant C/T snv 1.6E-05 30
rs6354
SLC6A4
0.732 0.280 17 30222880 5 prime UTR variant G/C;T snv 16
rs110402
CRHR1 ; LINC02210-CRHR1 ; MAPT-AS1
0.790 0.120 17 45802681 intron variant G/A;C snv 12
rs2020936
SLC6A4
0.776 0.160 17 30223796 intron variant G/A;C snv 10