Gene: ALK ×
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: rs1057519783
rs1057519783
ALK
10 0.851 0.080 2 29220747 missense variant C/T snv 0.040 1.000 4 2014 2019
dbSNP: rs1057519698
rs1057519698
ALK
8 0.827 0.120 2 29222347 missense variant A/G;T snv 0.030 1.000 3 2014 2016
dbSNP: rs1057519784
rs1057519784
ALK
7 0.827 0.080 2 29220765 missense variant G/T snv 0.020 1.000 2 2014 2017
dbSNP: rs281864719
rs281864719
ALK
14 0.763 0.240 2 29220831 missense variant A/C;G;T snv 0.020 1.000 2 2014 2017
dbSNP: rs1057519781
rs1057519781
ALK
9 0.807 0.160 2 29209816 missense variant C/G snv 0.010 1.000 1 2016 2016
dbSNP: rs113994088
rs113994088
ALK
4 0.925 0.080 2 29222584 missense variant C/G snv 0.010 1.000 1 2018 2018
dbSNP: rs113994091
rs113994091
ALK
4 0.882 0.160 2 29222407 missense variant G/A;C snv 3.2E-05 0.010 1.000 1 2017 2017
dbSNP: rs550608288
rs550608288
ALK
1 1.000 0.080 2 29717646 missense variant T/C snv 5.2E-05 0.010 1.000 1 2014 2014
dbSNP: rs751306825
rs751306825
ALK
4 0.925 0.080 2 29220759 missense variant G/A;T snv 4.0E-06 0.010 1.000 1 2017 2017
dbSNP: rs863225283
rs863225283
ALK
4 0.925 0.080 2 29213993 missense variant A/C snv 0.010 1.000 1 2016 2016
dbSNP: rs958335893
rs958335893
ALK
1 1.000 0.080 2 29193478 missense variant C/T snv 0.010 1.000 1 2015 2015