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: rs1980057
rs1980057 		6 1.000 0.040 4 144564586 intron variant C/T snv 0.31 0.700 1.000 2 2009 2010