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: rs150571175
rs150571175
TECPR2
1 1.000 14 102379530 intron variant G/A snv 8.4E-02 0.800 1.000 1 2014 2014
dbSNP: rs7705093
rs7705093
LNPEP
1 1.000 5 96954943 intron variant C/T snv 0.41 0.800 1.000 1 2014 2014