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: rs373849532
rs373849532
HINT1
1 1.000 0.080 5 131159494 missense variant G/T snv 1.6E-05 2.1E-05 0.800 1.000 2 2006 2012