rs3763317, BTNL2

N. diseases: 2
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
C4 complement assay (procedure)
CUI: C0577608
Disease: C4 complement assay (procedure)
15 1.000 0.040 6 32409011 upstream gene variant C/T snv 0.49 0.800 1.000 1 2012 2012
Cardiomyopathy, Familial Idiopathic
CUI: C1449563
Disease: Cardiomyopathy, Familial Idiopathic
243 1.000 0.040 6 32409011 upstream gene variant C/T snv 0.49 0.010 1.000 1 2015 2015