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Items: 9

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FMN2
(T269S)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
+1 more
GUncertain significance
FMN2
(S282R)
Single nucleotide variant
(missense variant)
not provided
GUncertain significance
FMN2
(S295P)
Single nucleotide variant
(missense variant)
not provided
GConflicting classifications of pathogenicity
FMN2
(G298D)
Single nucleotide variant
(missense variant)
not specified
+1 more
GBenign/Likely benign
FMN2
(L451Q)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign/Likely benign
FMN2
(P858T +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GConflicting classifications of pathogenicity
FMN2
(G945R +1 more)
Single nucleotide variant
(missense variant +1 more)
not specified
+1 more
GUncertain significance
FMN2
(P1044R +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
FMN2
(V1105E +1 more)
Single nucleotide variant
(missense variant +1 more)
not provided
GUncertain significance
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