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rs863224871

From SNPedia

ClinVar
Risk rs863224871(;)
Alt rs863224871(;)
Reference rs863224871(CGAGCAG;CGAGCAG)
Significance Probable-Pathogenic
Disease Infections
Variation info
Gene FADD
CLNDBN Infections, recurrent, with encephalopathy, hepatic dysfunction, and cardiovascular malformations
Reversed 0
HGVS NC_000011.9:g.70049617_70049623delAGCGAGC
CLNSRC
CLNACC RCV000195419.1,