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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
RXFP2
(R373Q +1 more)
Single nucleotide variant
(missense variant)
RXFP2-related disorder
GUncertain significance
RXFP2
(I452V +1 more)
Single nucleotide variant
(missense variant)
not specified
+1 more
GUncertain significance