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: rs11209026
rs11209026
46 0.597 0.680 1 67240275 missense variant G/A snv 4.2E-02 4.6E-02 0.900 0.944 36 2006 2020
dbSNP: rs7517847
rs7517847
19 0.689 0.600 1 67215986 intron variant T/G snv 0.37 0.880 1.000 11 2007 2019
dbSNP: rs1004819
rs1004819
9 0.776 0.360 1 67204530 intron variant G/A snv 0.30 0.860 1.000 8 2006 2019
dbSNP: rs10889677
rs10889677
40 0.627 0.720 1 67259437 3 prime UTR variant C/A snv 0.27 0.850 1.000 7 2006 2020
dbSNP: rs2201841
rs2201841
14 0.716 0.440 1 67228519 intron variant A/G;T snv 0.850 1.000 7 2006 2013
dbSNP: rs76418789
rs76418789
3 0.882 0.080 1 67182913 missense variant G/A snv 7.3E-03 4.5E-03 0.850 1.000 7 2011 2019
dbSNP: rs11805303
rs11805303
6 0.827 0.240 1 67209833 intron variant C/T snv 0.30 0.810 1.000 3 2007 2012
dbSNP: rs11465804
rs11465804
10 0.752 0.320 1 67236843 intron variant T/G snv 4.4E-02 5.4E-02 0.800 1.000 5 2006 2010
dbSNP: rs1343151
rs1343151
10 0.752 0.400 1 67253446 intron variant G/A snv 0.41 0.800 1.000 3 2006 2007
dbSNP: rs10889676
rs10889676
5 0.827 0.120 1 67256884 intron variant C/A;T snv 0.800 1.000 2 2007 2016
dbSNP: rs11465802
rs11465802
1 1.000 0.040 1 67219915 intron variant A/C;T snv 0.800 1.000 1 2007 2007
dbSNP: rs2064689
rs2064689
1 1.000 0.040 1 67187327 intron variant G/A snv 0.29 0.800 1.000 1 2007 2007
dbSNP: rs2902440
rs2902440
1 1.000 0.040 1 67205233 intron variant G/A snv 0.37 0.800 1.000 1 2007 2007
dbSNP: rs9988642
rs9988642
3 0.882 0.080 1 67260421 downstream gene variant T/C snv 0.13 0.800 1.000 1 2007 2007
dbSNP: rs10489629
rs10489629
5 0.827 0.240 1 67222666 intron variant T/C snv 0.48 0.700 1.000 1 2006 2006
dbSNP: rs11209008
rs11209008
3 0.882 0.080 1 67157615 intron variant G/A;T snv 5.7E-02 0.700 1.000 1 2007 2007
dbSNP: rs11580078
rs11580078
14 0.724 0.240 1 67203951 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs11581607
rs11581607
4 0.925 0.040 1 67242007 intron variant G/A snv 4.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs11804284
rs11804284
1 1.000 0.040 1 67233571 intron variant T/A;C;G snv 0.700 1.000 1 2007 2007
dbSNP: rs183686347
rs183686347
5 0.827 0.120 1 67237759 intron variant G/A snv 4.8E-03 0.700 1.000 1 2016 2016
dbSNP: rs7518660
rs7518660
2 0.925 0.120 1 67219760 intron variant G/A snv 0.43 0.47 0.700 1.000 1 2007 2007
dbSNP: rs7539625
rs7539625
1 1.000 0.040 1 67207082 intron variant G/A snv 0.33 0.30 0.700 1.000 1 2007 2007
dbSNP: rs80174646
rs80174646
5 0.827 0.120 1 67242472 intron variant G/T snv 5.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs1884444
rs1884444
34 0.637 0.600 1 67168129 missense variant G/T snv 0.52 0.51 0.020 1.000 2 2008 2013
dbSNP: rs1442094471
rs1442094471
1 1.000 0.040 1 67258910 missense variant T/A;C snv 0.010 1.000 1 2008 2008