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: rs104894339
rs104894339
AQP2 ; LOC101927318
4 0.851 0.080 12 49955577 missense variant C/G;T snv 5.0E-06; 5.5E-05 0.010 1.000 1 2004 2004