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: rs897876
rs897876 		4 0.882 0.040 2 65564447 intron variant C/T snv 0.30 0.010 1.000 1 2014 2014