"MAN2C1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2634552	NM_006715.4(MAN2C1):c.2584G>A (p.Gly862Ser)	MAN2C1, NEIL1 (G763S +2 more)	Single nucleotide variant (missense variant +2 more)	MAN2C1-related condition	GUncertain significance
Select item 2636037	NM_006715.4(MAN2C1):c.2164G>A (p.Val722Met)	MAN2C1 (V623M +2 more)	Single nucleotide variant (missense variant)	MAN2C1-related condition	GUncertain significance
Select item 3060879	NM_006715.4(MAN2C1):c.1460+9A>G	MAN2C1	Single nucleotide variant (intron variant)	MAN2C1-related condition	GBenign

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