Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs7574865
rs7574865
STAT4
59 0.574 0.720 2 191099907 intron variant T/G snv 0.79 0.810 1.000 3 2012 2014
dbSNP: rs6441286
rs6441286
IL12A-AS1
2 0.925 0.080 3 160011091 intron variant T/G snv 0.36 0.800 1.000 2 2009 2010
dbSNP: rs1003643
rs1003643 		1 1.000 0.080 22 39280489 downstream gene variant T/G snv 0.34 0.700 1.000 1 2011 2011
dbSNP: rs10237488
rs10237488
SDK1
1 1.000 0.080 7 4034710 intron variant T/G snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs11556218
rs11556218
IL16
27 0.653 0.600 15 81305928 missense variant T/G snv 9.6E-02 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12437560
rs12437560 		1 1.000 0.080 15 61832507 upstream gene variant T/G snv 0.20 0.700 1.000 1 2012 2012
dbSNP: rs13236009
rs13236009
TNPO3
1 1.000 0.080 7 129023119 intron variant T/G snv 9.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs1939697
rs1939697
CNTN5
1 1.000 0.080 11 100220961 intron variant T/G snv 0.81 0.700 1.000 1 2012 2012
dbSNP: rs2069443
rs2069443
CDK5 ; SLC4A2
2 1.000 0.080 7 151058086 intron variant T/G snv 0.32 0.010 1.000 1 2011 2011
dbSNP: rs2208397
rs2208397
RAD51B
1 1.000 0.080 14 68286570 intron variant T/G snv 0.68 0.700 1.000 1 2011 2011
dbSNP: rs2732649
rs2732649 		1 1.000 0.080 17 46267444 non coding transcript exon variant T/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs2866409
rs2866409
MANBA
1 1.000 0.080 4 102633104 intron variant T/G snv 0.55 0.700 1.000 1 2012 2012
dbSNP: rs3822659
rs3822659
WWC1
2 0.925 0.080 5 168431367 missense variant T/G snv 8.7E-02 0.12 0.010 1.000 1 2017 2017
dbSNP: rs4620530
rs4620530
CHRM3 ; CHRM3-AS1
2 0.925 0.080 1 239900521 intron variant T/G snv 0.44 0.010 1.000 1 2020 2020
dbSNP: rs480913
rs480913
IL12A-AS1
1 1.000 0.080 3 160011793 non coding transcript exon variant T/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs571099
rs571099
IL12A-AS1
1 1.000 0.080 3 160014777 intron variant T/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs586094
rs586094
IL12A-AS1
1 1.000 0.080 3 160011761 non coding transcript exon variant T/G snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs62062797
rs62062797
MAPT
1 1.000 0.080 17 45950000 intron variant T/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs62064663
rs62064663
MAPT
1 1.000 0.080 17 46002673 intron variant T/G snv 0.14 0.700 1.000 1 2012 2012
dbSNP: rs725613
rs725613
CLEC16A
4 0.851 0.240 16 11075826 intron variant T/G snv 0.42 0.700 1.000 1 2011 2011
dbSNP: rs3771317
rs3771317
NAB1
1 1.000 0.080 2 190679236 intron variant T/C;G snv 0.800 1.000 2 2011 2015
dbSNP: rs1726773
rs1726773
SPIB
1 1.000 0.080 19 50424313 intron variant T/C;G snv 0.700 1.000 1 2011 2011
dbSNP: rs2366643
rs2366643
LINC01100 ; IL12A-AS1
1 1.000 0.080 3 160018698 intron variant T/C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs34416056
rs34416056
MAPT-AS1
1 1.000 0.080 17 45873854 intron variant T/C;G snv 0.700 1.000 1 2012 2012
dbSNP: rs4780355
rs4780355
SOCS1 ; RMI2 ; LOC105371082
3 0.882 0.120 16 11254001 intron variant T/C;G snv 0.700 1.000 1 2012 2012