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Links from OMIM

Items: 3

Variation
Gene
(Protein Change)
Type
(Consequence)
ConditionClassification, Review status
FGF17
(N187S +1 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 20 with or without anosmia
GPathogenic
FGF17
(R177H +1 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 20 without anosmia
GPathogenic
FGF17
(I108T +1 more)
Single nucleotide variant
(missense variant)
Hypogonadotropic hypogonadism 20 with or without anosmia
Grisk factor
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