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: rs756205995
rs756205995
1 1.000 11 65187995 missense variant G/A;C snv 6.5E-05 0.800 1.000 1 2016 2016
dbSNP: rs375817528
rs375817528
25 0.776 0.160 11 65206824 splice region variant G/A snv 1.2E-04 1.2E-04 0.700 0
dbSNP: rs875989787
rs875989787
1 1.000 11 65206793 stop gained C/T snv 0.700 0
dbSNP: rs875989845
rs875989845
1 1.000 11 65183542 frameshift variant C/- delins 0.700 0
dbSNP: rs367610255
rs367610255
1 1.000 11 65209906 missense variant C/T snv 6.0E-05 3.5E-05 0.010 1.000 1 2019 2019