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: rs1110061
rs1110061
7 0.807 0.200 9 124500523 missense variant C/A;G snv 4.3E-06; 0.10 0.010 1.000 1 2005 2005
dbSNP: rs371701248
rs371701248
3 0.882 0.160 9 124491156 missense variant C/T snv 1.3E-04 5.6E-05 0.010 1.000 1 2007 2007