Source: ALL
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: rs79666294
rs79666294 		2 5 155047146 regulatory region variant C/T snv 2.2E-02 0.700 1.000 1 2018 2018