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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
MDM2
(L144P +1 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GConflicting classifications of pathogenicity
MDM2
(I211L +2 more)
Single nucleotide variant
(missense variant +1 more)
Inborn genetic diseases
+1 more
GUncertain significance
MDM2
(D105N +5 more)
Single nucleotide variant
(missense variant)
Inborn genetic diseases
GUncertain significance
MDM2
(Y209C +5 more)
Single nucleotide variant
(missense variant)
Accelerated tumor formation, susceptibility to
+1 more
GUncertain significance
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