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: rs121909520
rs121909520
2 0.925 0.080 1 229432660 missense variant T/C snv 0.010 1.000 1 2016 2016
dbSNP: rs1273559032
rs1273559032
1 1.000 0.080 1 229432619 missense variant C/T snv 0.010 1.000 1 2004 2004
dbSNP: rs267606626
rs267606626
1 1.000 0.080 1 229432788 missense variant C/A snv 0.010 1.000 1 2009 2009
dbSNP: rs267606627
rs267606627
1 1.000 0.080 1 229432787 missense variant G/A;T snv 0.010 1.000 1 2009 2009
dbSNP: rs886044062
rs886044062
1 1.000 0.080 1 229432087 missense variant C/T snv 0.010 1.000 1 2011 2011