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: rs13141641
rs13141641 		8 1.000 0.040 4 144585304 intron variant T/C snv 0.32 0.800 1.000 4 2012 2017