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: rs201095702
rs201095702
1 1.000 9 124500326 missense variant C/T snv 1.3E-04 7.0E-05 0.800 1.000 1 2010 2010
dbSNP: rs387906690
rs387906690
1 1.000 9 124500568 missense variant G/A snv 6.2E-05 2.1E-05 0.800 1.000 1 2010 2010
dbSNP: rs200749741
rs200749741
2 0.925 0.080 9 124500574 missense variant G/A snv 2.3E-04 9.3E-04 0.700 1.000 1 2010 2010
dbSNP: rs780568525
rs780568525
1 1.000 9 124500248 missense variant C/A;T snv 6.9E-05 0.700 1.000 1 2010 2010
dbSNP: rs1253324106
rs1253324106
1 1.000 9 124500389 missense variant G/A snv 1.3E-05 7.0E-06 0.700 0
dbSNP: rs200163795
rs200163795
2 0.925 0.080 9 124500592 missense variant C/G;T snv 2.3E-04; 4.1E-06 0.700 0