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: rs114540395
rs114540395 		1 1.000 0.040 10 101719305 intron variant C/T snv 9.2E-02 0.700 1.000 1 2015 2015