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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
A2ML1
(F296S +1 more)
Single nucleotide variant
(missense variant)
not specified
GUncertain significance
A2ML1
(R1122W +1 more)
Single nucleotide variant
(missense variant)
not specified
+2 more
GBenign
A2ML1
Single nucleotide variant
(splice donor variant)
Otitis media, susceptibility to
+2 more
GConflicting classifications of pathogenicity
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