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: rs11568821
rs11568821
10 0.827 0.200 2 241851760 intron variant C/G;T snv 0.010 1.000 1 2018 2018
dbSNP: rs36084323
rs36084323
8 0.807 0.280 2 241859444 upstream gene variant C/T snv 5.4E-02 0.010 1.000 1 2018 2018