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: rs1437969513
rs1437969513
1 1.000 0.040 6 1611203 missense variant C/T snv 1.1E-05 0.010 1.000 1 2006 2006
dbSNP: rs77888940
rs77888940
1 1.000 0.040 6 1610017 5 prime UTR variant C/A;G;T snv 0.010 1.000 1 2016 2016
dbSNP: rs79691946
rs79691946
2 0.925 0.040 6 1611334 missense variant C/T snv 2.8E-03 3.0E-02 0.010 1.000 1 2016 2016
dbSNP: rs886041355
rs886041355
1 1.000 0.040 6 1610901 stop gained G/A snv 0.010 1.000 1 2006 2006