Related gene-specific medical variations for Gene (Select 84501) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3169212	NM_032451.2(SPIRE2):c.20G>C (p.Cys7Ser)	LOC130059841, SPIRE2 (C7S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542635	NM_032451.2(SPIRE2):c.41C>A (p.Ala14Glu)	LOC130059841, SPIRE2 (A14E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241888	NM_032451.2(SPIRE2):c.68C>G (p.Ser23Cys)	LOC130059841, SPIRE2 (S23C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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