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: rs104893677
rs104893677
2 0.923 0.179 3 148741880 missense variant C/T snp 0.700 1 2005 2005
dbSNP: rs121917742
rs121917742
REN
2 0.923 0.179 1 204159399 missense variant C/T snp 4.0E-06 0.700 1 2005 2005
dbSNP: rs74315283
rs74315283
AGT
2 0.923 0.179 1 230705933 missense variant C/A,T snp 8.0E-06; 2.4E-05 3.2E-05 0.700 1 2005 2005
dbSNP: rs868694193
rs868694193
REN
2 0.923 0.179 1 204161355 missense variant C/T snp 4.1E-06 0.700 1 2005 2005