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: rs115466046
rs115466046
2 1 160042480 missense variant C/T snv 1.2E-02 1.1E-02 0.010 1.000 1 2011 2011
dbSNP: rs140646329
rs140646329
2 1 160042283 missense variant C/T snv 2.0E-05 1.4E-05 0.010 1.000 1 2011 2011