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Items: 2

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGFR1
(W577R +7 more)
Single nucleotide variant
(missense variant)
Hartsfield-Bixler-Demyer syndrome
GPathogenic
FGFR1
(E478fs +7 more)
Deletion
(frameshift variant)
Hypogonadotropic hypogonadism 2 with or without anosmia
GPathogenic