"CD52-related disorder"[Disease/phenotype] AND "PreventionGenetics, pa - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3057395	NM_001803.3(CD52):c.12C>T (p.Phe4=)	CD52, LOC129929813 +1 more	Single nucleotide variant (synonymous variant +1 more)	CD52-related disorder	GLikely benign
Select item 3059084	NM_001803.3(CD52):c.119A>G (p.Asn40Ser)	CD52 (N40S)	Single nucleotide variant (missense variant)	CD52-related disorder	GBenign
Select item 3059585	NM_001803.3(CD52):c.123A>G (p.Ile41Met)	CD52 (I41M)	Single nucleotide variant (missense variant)	CD52-related disorder	GBenign

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