"GenomeConnect, ClinGen"[submitter] AND "LOC126863014"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 338170	NM_006892.4(DNMT3B):c.1572T>C (p.Cys524=)	DNMT3B, LOC126863014	Single nucleotide variant (synonymous variant)	Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency +2 more	GBenign
Select item 338171	NM_006892.4(DNMT3B):c.1674T>C (p.Tyr558=)	DNMT3B, LOC126863014	Single nucleotide variant (synonymous variant)	Centromeric instability of chromosomes 1,9 and 16 and immunodeficiency +2 more	GBenign