Details for Combination OLI1779

VARIANTS NOD2:c.2104C>T, p.Arg702Trp in Heterozygous form; NOD2:c.2863G>A, p.Val955Ile in Heterozygous form; NLRP3:c.2107C>A, p.Gln703Lys in Heterozygous form; NLRP12:c.1206C>G, p.Phe402Leu in Heterozygous form
GENE COMBINATION NLRP12; NLRP3; NOD2
OLIGOGENIC EFFECT Unknown
ETHNICITY European/Caucasian
OMIM IDS N.A.
DISEASES Autoinflammatory syndrome
REFERENCES 37928541
SCORES
FAMmanual
0

STAT
manualknowledgemeta
200

GENE
manualmanual harmonizedknowledgemeta
2202

VAR
manualknowledgemeta
000

FUN
manualmeta
00

FINAL
manualmeta
00


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