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: rs146013446
rs146013446
2 0.925 4 105437964 missense variant C/T snv 4.9E-04 6.9E-04 0.800 1.000 1 2016 2016
dbSNP: rs138215926
rs138215926
1 1.000 4 105399137 missense variant G/A snv 2.0E-04 4.3E-04 0.700 0