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: rs121908280
rs121908280
RAX2
1 1.000 0.040 19 3770916 missense variant C/A;G;T snv 6.2E-06; 1.2E-04 0.800 1.000 1 2004 2004