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: rs2066844
rs2066844
NOD2
54 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 0.010 1.000 1 2008 2008
dbSNP: rs763035
rs763035 		1 1.000 0.040 6 32427068 intergenic variant G/A snv 0.13 0.010 1.000 1 2015 2015