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: rs202247795
rs202247795
1 1.000 0.040 2 211702102 missense variant C/T snv 0.700 1.000 1 2009 2009
dbSNP: rs267599192
rs267599192
1 1.000 0.040 2 211673250 missense variant G/A snv 0.700 1.000 1 2009 2009
dbSNP: rs267599193
rs267599193
1 1.000 0.040 2 211713583 missense variant C/T snv 0.700 1.000 1 2009 2009
dbSNP: rs535202189
rs535202189
1 1.000 0.040 2 211673256 missense variant C/T snv 6.8E-05 0.700 1.000 1 2009 2009
dbSNP: rs55671017
rs55671017
1 1.000 0.040 2 211705339 missense variant G/A;T snv 8.0E-06; 6.4E-04 0.700 1.000 1 2009 2009
dbSNP: rs776347334
rs776347334
1 1.000 0.040 2 211430974 missense variant C/T snv 1.2E-05 0.700 1.000 1 2009 2009