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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
HNRNPR
(P443L +6 more)
Single nucleotide variant
(missense variant)
HNRNPR-related disorder
GUncertain significance
HNRNPR
(V79fs)
Deletion
(5 prime UTR variant +1 more)
HNRNPR-related disorder
GUncertain significance