Gene: AHSG ×
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: rs35457250
rs35457250
AHSG
5 0.925 0.080 3 186620775 missense variant C/T snv 9.0E-03 8.1E-03 0.010 1.000 1 2005 2005
dbSNP: rs4917
rs4917
AHSG
9 0.790 0.160 3 186619924 missense variant T/C snv 0.68 0.68 0.010 1.000 1 2005 2005
dbSNP: rs4918
rs4918
AHSG
12 0.763 0.400 3 186620593 missense variant G/A;C snv 0.67 0.010 1.000 1 2005 2005
dbSNP: rs70961709
rs70961709
AHSG
3 1.000 0.040 3 186620652 missense variant G/A;C snv 4.0E-06; 4.0E-06 0.010 1.000 1 2005 2005