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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CIROP
(H609Q +1 more)
Single nucleotide variant
(missense variant)
CIROP-related condition
GLikely benign
CIROP
(S31F)
Single nucleotide variant
(missense variant)
CIROP-related condition
GLikely benign