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Links from Gene

Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
LOC129996327, RNF8
(W29C)
Single nucleotide variant
(missense variant +1 more)
not specified
GUncertain significance
ILRUN-AS1, IP6K3
+2582 more
Copy number gain
See cases
GPathogenic