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: rs5743277
rs5743277
NOD2
2 1.000 0.040 16 50712018 missense variant C/G;T snv 1.2E-05; 3.2E-03 0.010 1.000 1 2015 2015