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: rs6435862
rs6435862
3 1.000 0.071 2 214807822 intron variant G/A,C,T snp 0.75 0.830 1.000 3 2010 2016
dbSNP: rs3768716
rs3768716
2 1.000 0.071 2 214771070 intron variant T/C snp 0.15 0.820 1.000 3 2010 2016
dbSNP: rs110419
rs110419
2 1.000 0.071 11 8231306 intron variant A/G snp 0.42 0.810 1.000 3 2011 2016
dbSNP: rs17065417
rs17065417
2 1.000 0.071 6 104958399 intron variant A/C snp 9.4E-02 0.810 1.000 2 2012 2017
dbSNP: rs6441201
rs6441201
3 0.923 0.071 3 158460535 intron variant G/A snp 0.50 0.810 1.000 2 2017 2018
dbSNP: rs6939340
rs6939340
3 1.000 0.071 6 22139775 intron variant A/G snp 0.62 0.810 1.000 1 2008 2008
dbSNP: rs281864719
rs281864719
ALK
10 0.846 0.143 2 29220831 missense variant A/C,G,T snp 0.800 1.000 18 1990 2016
dbSNP: rs863225281
rs863225281
ALK
9 0.821 0.143 2 29220829 missense variant G/C,T snp 0.800 1.000 17 2008 2016
dbSNP: rs4712653
rs4712653
1 6 22125735 intron variant T/C,G snp 0.60; 3.2E-05 0.800 3 2008 2017
dbSNP: rs17487792
rs17487792
1 2 214778776 intron variant C/T snp 0.15 0.800 2 2010 2017
dbSNP: rs7587476
rs7587476
1 2 214789163 intron variant T/A,C snp 0.75 0.800 2 2010 2012
dbSNP: rs9295536
rs9295536
1 6 22131700 intron variant C/A snp 0.58 0.800 2 2008 2012
dbSNP: rs11037575
rs11037575
1 11 43706780 intron variant T/C snp 0.38 0.800 1 2012 2012
dbSNP: rs4336470
rs4336470
1 6 104732910 intron variant C/T snp 0.44 0.800 1 2012 2012
dbSNP: rs113994087
rs113994087
ALK
6 1.000 0.071 2 29209798 missense variant C/A,T snp 0.740 1.000 9 2008 2016
dbSNP: rs35850753
rs35850753
4 0.878 0.071 17 7675353 5 prime UTR variant C/T snp 1.9E-02 0.710 1.000 2 2014 2017
dbSNP: rs3796727
rs3796727
CPZ
3 0.923 0.071 4 8611299 intron variant G/A snp 0.26 0.34 0.710 1.000 2 2017 2018
dbSNP: rs1057519697
rs1057519697
ALK
1 2 29220830 missense variant A/C snp 0.700 4 2008 2016
dbSNP: rs1057519698
rs1057519698
ALK
1 2 29222347 missense variant A/T snp 0.700 3 2008 2012
dbSNP: rs281864720
rs281864720
ALK
5 1.000 0.036 2 29213994 missense variant A/C,G,T snp 0.700 3 2008 2012
dbSNP: rs863225285
rs863225285
ALK
2 2 29209789 missense variant T/G snp 0.700 3 2008 2012
dbSNP: rs113994091
rs113994091
ALK
2 2 29222407 missense variant G/A,C snp 3.2E-05 6.4E-05 0.700 2 2012 2012
dbSNP: rs121908163
rs121908163
2 1 10345943 missense variant C/T snp 2.0E-04 3.2E-05 0.700 2 2008 2015
dbSNP: rs863225283
rs863225283
ALK
3 1.000 0.071 2 29213993 missense variant A/C snp 0.700 2 2012 2012
dbSNP: rs863225284
rs863225284
ALK
2 2 29213992 missense variant G/C,T snp 0.700 2 2012 2012