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: rs10818684
rs10818684 		2 1.000 0.040 9 122407651 intron variant C/T snv 0.62 0.010 1.000 1 2014 2014