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: rs754041352
rs754041352
1 1.000 0.080 19 43552051 missense variant G/A snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs25487
rs25487
205 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 0.100 0.833 24 2004 2016
dbSNP: rs1799782
rs1799782
151 0.474 0.800 19 43553422 missense variant G/A snv 9.5E-02 7.0E-02 0.100 0.857 14 2009 2016
dbSNP: rs25489
rs25489
78 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 0.040 1.000 4 2010 2013
dbSNP: rs774388757
rs774388757
1 1.000 0.080 19 43553421 missense variant C/T snv 2.0E-05 4.2E-05 0.010 1.000 1 2013 2013