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: rs12509636
rs12509636 		1 1.000 0.080 4 105089276 intron variant C/T snv 0.39 0.700 1.000 1 2017 2017