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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
CHD7
(R1741C)
Single nucleotide variant
(missense variant +1 more)
CHARGE syndrome
GUncertain significance
CHD7
(M2699fs +1 more)
Deletion
(frameshift variant)
Hypogonadotropic hypogonadism 5 with or without anosmia
GLikely pathogenic