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: rs11030108
rs11030108
1 1.000 0.036 11 27673917 intron variant A/G snp 0.73 0.010 1.000 1 2014 2014
dbSNP: rs1157659
rs1157659
1 1.000 0.036 11 27736075 intron variant A/G snp 0.39 0.010 1.000 1 2014 2014
dbSNP: rs115881343
rs115881343
1 1.000 0.036 19 44899959 intron variant C/T snp 2.9E-02 0.010 1.000 1 2014 2014
dbSNP: rs1256065
rs1256065
1 1.000 0.036 14 64232214 3 prime UTR variant G/T snp 0.66 0.010 1.000 1 2009 2009
dbSNP: rs13133980
rs13133980
1 1.000 0.036 4 41000929 intron variant G/A,C,T snp 0.49 0.010 1.000 1 2013 2013
dbSNP: rs1557372
rs1557372
1 1.000 0.036 21 41460614 regulatory region variant C/T snp 0.39 0.010 1.000 1 2013 2013
dbSNP: rs17601241
rs17601241
1 1.000 0.036 15 51215677 intron variant G/A snp 0.11 7.6E-02 0.010 1.000 1 2009 2009
dbSNP: rs199778549
rs199778549
1 1.000 0.036 20 63349990 missense variant G/C snp 6.7E-05 0.010 1.000 1 2012 2012
dbSNP: rs267606663
rs267606663
1 1.000 0.036 19 44909021 missense variant G/A,C snp 7.3E-06 3.2E-05 0.010 1.000 1 2012 2012
dbSNP: rs457274
rs457274
MX1
1 1.000 0.036 21 41420558 5 prime UTR variant C/G snp 0.35 0.010 1.000 1 2013 2013
dbSNP: rs469083
rs469083
MX1
1 1.000 0.036 21 41436789 intron variant C/T snp 0.61 0.010 1.000 1 2013 2013
dbSNP: rs564919438
rs564919438
1 1.000 0.036 1 45332421 stop gained G/C,T snp 8.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs6439886
rs6439886
1 1.000 0.036 3 139963653 intron variant A/G snp 0.14 0.010 1.000 1 2012 2012
dbSNP: rs6853
rs6853
1 1.000 0.036 3 38142879 3 prime UTR variant A/G snp 0.15 0.010 1.000 1 2016 2016
dbSNP: rs728524
rs728524
1 1.000 0.036 6 151982302 intron variant A/G,T snp 9.5E-02 0.010 1.000 1 2009 2009
dbSNP: rs772720363
rs772720363
1 1.000 0.036 20 63350819 missense variant C/T snp 4.0E-06 0.010 1.000 1 2012 2012
dbSNP: rs7759295
rs7759295
1 1.000 0.036 6 41168112 intergenic variant C/G,T snp 8.9E-02 0.010 1.000 1 2015 2015
dbSNP: rs8179176
rs8179176
1 1.000 0.036 6 151842199 intron variant C/A snp 0.010 1.000 1 2009 2009
dbSNP: rs1187120
rs1187120
2 0.923 0.036 6 34182850 regulatory region variant T/C snp 0.99 0.010 1.000 1 2016 2016
dbSNP: rs1938526
rs1938526
2 0.923 0.036 10 60540625 intron variant A/G snp 9.4E-02 0.010 1.000 1 2015 2015
dbSNP: rs2731880
rs2731880
2 0.923 0.036 5 36603282 intergenic variant T/C snp 0.53 0.010 1.000 1 2015 2015
dbSNP: rs4354668
rs4354668
2 0.923 0.036 11 35419429 5 prime UTR variant T/G snp 0.53 0.010 1.000 1 2015 2015
dbSNP: rs6910730
rs6910730
2 1.000 0.036 6 41278895 intron variant A/G snp 0.21 0.010 1.000 1 2015 2015
dbSNP: rs9877502
rs9877502
2 0.923 0.071 3 190951729 intergenic variant G/A snp 0.40 0.010 1.000 1 2013 2013
dbSNP: rs112422930
rs112422930
3 0.878 0.143 1 45332409 missense variant A/C snp 0.010 1.000 1 2012 2012