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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MMAB
(R186G)
Single nucleotide variant
(missense variant +1 more)
Methylmalonic aciduria, cblB type
GUncertain significance
MMAB, MVK
(L27F)
Single nucleotide variant
(missense variant +1 more)
not provided
+2 more
GUncertain significance
MMAB, MVK
(G23D)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+2 more
GUncertain significance
MVK, MMAB
(C4R)
Single nucleotide variant
(missense variant +1 more)
Methylmalonic aciduria, cblB type
GConflicting classifications of pathogenicity
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