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: rs104894714
rs104894714
PRX
2 0.925 0.080 19 40395495 stop gained G/A snv 3.2E-05 0.700 1.000 1 2001 2001
dbSNP: rs104894706
rs104894706
PRX
2 0.925 0.080 19 40397766 stop gained G/A;C;T snv 0.700 0
dbSNP: rs104894708
rs104894708
PRX
5 0.851 0.120 19 40395144 stop gained G/A snv 8.0E-06 0.700 0
dbSNP: rs1385904344
rs1385904344
PRX
1 1.000 19 40394649 stop gained C/A;T snv 4.1E-06 1.4E-05 0.700 0
dbSNP: rs1568708792
rs1568708792
PRX
1 1.000 19 40397373 frameshift variant C/- delins 0.700 0
dbSNP: rs281865061
rs281865061
PRX
1 1.000 19 40398754 frameshift variant G/- delins 0.700 0
dbSNP: rs281865062
rs281865062
PRX
1 1.000 19 40396254 frameshift variant C/- delins 0.700 0
dbSNP: rs3814290
rs3814290
PRX
1 1.000 19 40396401 missense variant C/A;G;T snv 4.0E-06; 9.2E-05 0.700 0