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: rs121909349
rs121909349
3 0.882 0.040 20 35434297 missense variant A/C snv 0.800 1.000 3 2005 2008
dbSNP: rs74315388
rs74315388
3 0.882 0.080 20 35434102 missense variant C/A;T snv 0.800 1.000 3 2005 2008
dbSNP: rs74315389
rs74315389
2 0.925 0.080 20 35433944 missense variant C/T snv 8.0E-06 1.4E-05 0.800 1.000 3 2005 2008