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: rs61755815
rs61755815
PRPH2
4 0.851 0.080 6 42704463 missense variant T/G snv 0.010 1.000 1 1996 1996
dbSNP: rs62645926
rs62645926
PRPH2
4 0.851 0.080 6 42721784 missense variant T/G snv 0.010 1.000 1 1996 1996