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: rs398124654
rs398124654
1 1.000 20 14326491 missense variant T/C snv 0.800 1.000 1 2013 2013
dbSNP: rs398124651
rs398124651
2 1.000 20 14327217 missense variant T/C snv 0.700 1.000 1 2013 2013
dbSNP: rs398124652
rs398124652
2 1.000 20 14327076 missense variant C/A snv 0.700 1.000 1 2013 2013
dbSNP: rs398124653
rs398124653
2 1.000 20 14327302 missense variant G/T snv 2.8E-05 2.1E-05 0.700 1.000 1 2013 2013