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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NOD2
(T189M +1 more)
Single nucleotide variant
(missense variant +1 more)
Blau syndrome
+4 more
GConflicting classifications of pathogenicity
NOD2
(L248R +1 more)
Single nucleotide variant
(missense variant +1 more)
Blau syndrome
+3 more
GConflicting classifications of pathogenicity
NOD2
(R791Q +1 more)
Single nucleotide variant
(missense variant +1 more)
Blau syndrome
+4 more
GConflicting classifications of pathogenicity
NOD2
(G978E +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
+3 more
GUncertain significance
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