"Women's Health and Genetics/Laboratory Corporation of America, LabCor - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063882	NM_002430.3(MN1):c.3048G>C (p.Leu1016Phe)	MN1 (L1016F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 981070	NM_002430.3(MN1):c.113C>A (p.Ala38Asp)	MN1 (A38D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2503984	NM_002430.3(MN1):c.36C>A (p.Asn12Lys)	MN1 (N12K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 981085	NM_002430.3(MN1):c.25C>G (p.Pro9Ala)	MN1 (P9A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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