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: rs180177173
rs180177173
AGXT
1 1.000 0.160 2 240869004 missense variant G/A;C snv 2.5E-05; 4.1E-06 0.800 1.000 2 2007 2012