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: rs387907053
rs387907053
HEPACAM ; LOC107984406
2 0.925 0.200 11 124924890 missense variant C/T snv 0.800 1.000 1 2011 2011
dbSNP: rs387907055
rs387907055
HEPACAM ; LOC107984406
2 0.925 0.200 11 124924881 missense variant G/A snv 0.800 1.000 1 2011 2011
dbSNP: rs149782549
rs149782549
HEPACAM ; LOC107984406
1 1.000 11 124922760 missense variant G/A snv 4.3E-04 5.3E-04 0.700 1.000 1 2011 2011
dbSNP: rs387907054
rs387907054
HEPACAM ; LOC107984406
2 0.925 11 124924889 missense variant C/T snv 0.700 1.000 1 2011 2011
dbSNP: rs1555055028
rs1555055028
HEPACAM ; LOC107984406
5 0.882 0.160 11 124923996 missense variant G/A snv 0.700 0