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: rs3877899
rs3877899
SELENOP ; CCDC152
7 0.827 0.160 5 42801166 missense variant C/A;T snv 4.0E-06; 0.20 0.010 1.000 1 2014 2014
dbSNP: rs7579
rs7579
SELENOP ; CCDC152
6 0.807 0.200 5 42800706 3 prime UTR variant C/T snv 0.31 0.26 0.010 1.000 1 2014 2014