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: rs12731372
rs12731372 		3 1 118310352 regulatory region variant C/T snv 0.19 0.700 1.000 1 2017 2017