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Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
NHP2, RMND5B
(P82L)
Single nucleotide variant
(missense variant +2 more)
Dyskeratosis congenita, autosomal recessive 1
+3 more
GBenign/Likely benign
NHP2, RMND5B
Single nucleotide variant
(3 prime UTR variant +1 more)
Dyskeratosis congenita, autosomal recessive 2
+2 more
GBenign/Likely benign
NHP2
(V64M)
Single nucleotide variant
(missense variant)
not specified
+4 more
GUncertain significance
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