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: rs104894029
rs104894029
NT5C3A
2 0.925 0.080 7 33015741 missense variant C/G snv 0.010 1.000 1 2005 2005