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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF8
(H182fs +4 more)
Duplication
(frameshift variant)
Hypogonadotropic hypogonadism 6 with or without anosmia
GLikely pathogenic
FGF8
(S87R +3 more)
Single nucleotide variant
(5 prime UTR variant +1 more)
not specified
GUncertain significance