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: rs113994087
rs113994087
ALK
12 0.827 0.120 2 29209798 missense variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs113994088
rs113994088
ALK
4 0.925 0.080 2 29222584 missense variant C/G snv 0.700 1.000 1 2011 2011
dbSNP: rs113994089
rs113994089
ALK
4 0.925 0.120 2 29220776 missense variant C/G;T snv 0.700 1.000 1 2011 2011