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: rs1800414
rs1800414
4 0.851 0.200 15 27951891 missense variant T/A;C snv 4.0E-06; 4.5E-02 0.010 1.000 1 2011 2011
dbSNP: rs74653330
rs74653330
5 0.851 0.200 15 27983407 missense variant C/T snv 8.4E-03 6.2E-03 0.010 1.000 1 2011 2011