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: rs80356726
rs80356726
12 0.763 0.120 1 11022352 splice acceptor variant G/A snv 4.0E-06 0.010 1.000 1 2011 2011
dbSNP: rs80356730
rs80356730
7 0.807 0.120 1 11022418 missense variant A/G snv 8.0E-06 0.010 1.000 1 2014 2014
dbSNP: rs80356731
rs80356731
3 0.882 0.080 1 11022437 missense variant A/G snv 0.010 1.000 1 2015 2015
dbSNP: rs80356732
rs80356732
2 0.925 0.080 1 11022444 missense variant C/A snv 8.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs80356733
rs80356733
7 0.790 0.200 1 11022451 missense variant G/T snv 0.010 1.000 1 2011 2011