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: rs638704
rs638704 		1 1.000 1 170629046 intron variant C/T snv 0.64 0.700 1.000 1 2018 2018