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: rs4407312
rs4407312
CST2
1 1.000 0.080 20 23826391 intron variant A/C;G;T snv 0.76; 4.1E-06; 6.6E-05 0.700 1.000 1 2011 2011