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: rs267607187
rs267607187
IQSEC2
1 1.000 0.080 X 53248778 missense variant T/G snv 0.800 1.000 2 2010 2015
dbSNP: rs267607188
rs267607188
IQSEC2
1 1.000 0.080 X 53254856 missense variant G/A snv 0.800 1.000 2 2010 2015
dbSNP: rs267607189
rs267607189
IQSEC2
1 1.000 0.080 X 53250303 missense variant C/T snv 0.800 1.000 2 2010 2015
dbSNP: rs875989799
rs875989799
IQSEC2
1 1.000 0.080 X 53248814 missense variant G/A snv 0.800 1.000 2 2010 2015