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: rs746055479
rs746055479
1 1.000 0.200 16 50712108 missense variant G/A;T snv 2.4E-05 0.700 0
dbSNP: rs752615209
rs752615209
1 1.000 0.200 16 50710956 missense variant C/G;T snv 8.0E-06 0.700 0
dbSNP: rs886040969
rs886040969
1 1.000 0.200 16 50712357 missense variant G/A snv 0.700 0
dbSNP: rs2066844
rs2066844
54 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 0.020 1.000 2 2009 2019
dbSNP: rs2066845
rs2066845
46 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 0.010 1.000 1 2009 2009
dbSNP: rs758548184
rs758548184
5 0.851 0.240 16 50699557 missense variant G/C snv 0.010 1.000 1 2008 2008