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: rs11176001
rs11176001 		3 12 66015587 regulatory region variant C/A snv 9.6E-02 0.700 1.000 2 2019 2019