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: rs1555055028
rs1555055028
HEPACAM ; LOC107984406
5 0.882 0.160 11 124923996 missense variant G/A snv 0.800 1.000 1 2011 2011
dbSNP: rs387907049
rs387907049
HEPACAM ; LOC107984406
1 1.000 11 124923851 missense variant G/A;T snv 8.0E-06; 4.0E-06 0.800 1.000 1 2011 2011
dbSNP: rs387907050
rs387907050
HEPACAM ; LOC107984406
2 0.925 0.200 11 124924880 missense variant C/T snv 0.800 1.000 1 2011 2011
dbSNP: rs387907051
rs387907051
HEPACAM ; LOC107984406
1 1.000 11 124923807 missense variant C/T snv 0.800 1.000 1 2011 2011
dbSNP: rs387907052
rs387907052
HEPACAM ; LOC107984406
1 1.000 11 124924863 missense variant G/A snv 0.800 1.000 1 2011 2011