Related gene-specific medical variations for Gene (Select 14) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3133470	NM_001087.5(AAMP):c.58A>G (p.Ser20Gly)	AAMP, LOC129935593 (S20G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3133351	NM_001087.5(AAMP):c.43C>A (p.Pro15Thr)	AAMP, LOC129935593 (P15T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462086	NM_001087.5(AAMP):c.44C>A (p.Pro15Gln)	AAMP, LOC129935593 (P15Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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