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: rs387906894
rs387906894
CORIN
1 1.000 4 47683803 missense variant T/C snv 4.0E-06 0.800 1.000 1 2012 2012
dbSNP: rs387906895
rs387906895
CORIN
1 1.000 4 47665207 missense variant T/C snv 0.800 1.000 1 2012 2012