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: rs104893858
rs104893858
5 0.827 0.080 4 110621214 missense variant T/C;G snv 8.0E-06 0.010 1.000 1 2001 2001
dbSNP: rs104893859
rs104893859
3 0.925 0.080 4 110618669 missense variant C/G;T snv 0.010 1.000 1 2011 2011
dbSNP: rs104893951
rs104893951
5 0.851 0.080 6 1610780 missense variant T/A;C snv 8.0E-06 0.010 1.000 1 2003 2003
dbSNP: rs121909338
rs121909338
2 0.925 0.080 6 1610833 missense variant C/T snv 0.010 1.000 1 2007 2007
dbSNP: rs1231780527
rs1231780527
2 0.925 0.080 10 101228551 missense variant C/T snv 6.5E-06 0.010 1.000 1 2001 2001
dbSNP: rs28936409
rs28936409
2 1.000 0.080 4 110621303 missense variant C/A;G;T snv 4.0E-06; 8.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs387906810
rs387906810
3 0.882 0.080 4 110618679 missense variant T/C snv 0.010 1.000 1 2001 2001