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Links from Gene

Items: 5

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RNF216
Duplication
not provided
GLikely pathogenic
RNF216
(E491D +1 more)
Single nucleotide variant
(missense variant)
Cerebellar ataxia-hypogonadism syndrome
GUncertain significance
RNF216
(M1fs)
Deletion
(frameshift variant +1 more)
Cerebellar ataxia-hypogonadism syndrome
GUncertain significance
RNF216
(C18W)
Single nucleotide variant
(missense variant)
Cerebellar ataxia-hypogonadism syndrome
GUncertain significance
RNF216
Copy number gain
not provided
GUncertain significance
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