Related gene-specific medical variations for Gene (Select 81848) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2582723	NM_001127496.3(SPRY4):c.278G>A (p.Ser93Asn)	SPRY4 (S116N +1 more)	Single nucleotide variant (missense variant)	Hypogonadotropic hypogonadism 17 with or without anosmia	GUncertain significance
Select item 1344747	NM_001127496.3(SPRY4):c.206G>T (p.Gly69Val)	SPRY4 (G69V +1 more)	Single nucleotide variant (missense variant)	Amenorrhea	GUncertain significance