Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7574865
STAT4
0.574 0.720 2 191099907 intron variant T/G snv 0.79 59
rs11556218
IL16
0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 27
rs725613
CLEC16A
0.851 0.240 16 11075826 intron variant T/G snv 0.42 4
rs2069443
SLC4A2 ; CDK5
1.000 0.080 7 151058086 intron variant T/G snv 0.32 2
rs3822659
WWC1
0.925 0.080 5 168431367 missense variant T/G snv 8.7E-02 0.12 2
rs4620530
CHRM3 ; CHRM3-AS1
0.925 0.080 1 239900521 intron variant T/G snv 0.44 2
rs6441286
IL12A-AS1
0.925 0.080 3 160011091 intron variant T/G snv 0.36 2
rs1003643 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 1
rs10237488
SDK1
1.000 0.080 7 4034710 intron variant T/G snv 0.33 1
rs12437560 1.000 0.080 15 61832507 upstream gene variant T/G snv 0.20 1
rs13236009
TNPO3
1.000 0.080 7 129023119 intron variant T/G snv 9.0E-02 1
rs1939697
CNTN5
1.000 0.080 11 100220961 intron variant T/G snv 0.81 1
rs2208397
RAD51B
1.000 0.080 14 68286570 intron variant T/G snv 0.68 1
rs2732649 1.000 0.080 17 46267444 non coding transcript exon variant T/G snv 0.14 1
rs2866409
MANBA
1.000 0.080 4 102633104 intron variant T/G snv 0.55 1
rs480913
IL12A-AS1
1.000 0.080 3 160011793 non coding transcript exon variant T/G snv 0.41 1
rs571099
IL12A-AS1
1.000 0.080 3 160014777 intron variant T/G snv 0.41 1
rs586094
IL12A-AS1
1.000 0.080 3 160011761 non coding transcript exon variant T/G snv 0.41 1
rs62062797
MAPT
1.000 0.080 17 45950000 intron variant T/G snv 0.14 1
rs62064663
MAPT
1.000 0.080 17 46002673 intron variant T/G snv 0.14 1
rs4780355
SOCS1 ; RMI2 ; LOC105371082
0.882 0.120 16 11254001 intron variant T/C;G snv 3
rs7503377
CDK12
1.000 0.080 17 39552588 intron variant T/C;G snv 2
rs1726773
SPIB
1.000 0.080 19 50424313 intron variant T/C;G snv 1
rs2366643
IL12A-AS1 ; LINC01100
1.000 0.080 3 160018698 intron variant T/C;G snv 1
rs34416056
MAPT-AS1
1.000 0.080 17 45873854 intron variant T/C;G snv 1