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Items: 4

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RNF216
(E491D +1 more)
Single nucleotide variant
(missense variant)
Cerebellar ataxia-hypogonadism syndrome
GUncertain significance
RNF216
(R28Q)
Single nucleotide variant
(missense variant)
not provided
+1 more
GConflicting classifications of pathogenicity
RNF216
(C18W)
Single nucleotide variant
(missense variant)
Cerebellar ataxia-hypogonadism syndrome
GUncertain significance
RNF216
(M1fs)
Deletion
(frameshift variant +1 more)
Cerebellar ataxia-hypogonadism syndrome
GUncertain significance
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