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: rs10035360
rs10035360 		1 1.000 0.080 5 34604531 regulatory region variant C/T snv 0.19 0.700 1.000 1 2009 2009