Related gene-specific medical variations for Gene (Select 284759) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2652134	NM_001122962.2(SIRPB2):c.555C>T (p.Asp185=)	LOC126862951, SIRPB2	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2611339	NM_001122962.2(SIRPB2):c.715A>G (p.Thr239Ala)	LOC126862951, SIRPB2 (T239A +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522000	NM_001122962.2(SIRPB2):c.515C>T (p.Thr172Ile)	LOC126862951, SIRPB2 (T172I +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2307344	NM_001122962.2(SIRPB2):c.460G>T (p.Asp154Tyr)	LOC126862951, SIRPB2 (D56Y +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2302505	NM_001122962.2(SIRPB2):c.652G>A (p.Val218Met)	SIRPB2, LOC126862951 (V120M +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2259861	NM_001122962.2(SIRPB2):c.679A>G (p.Ile227Val)	LOC126862951, SIRPB2 (I129V +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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