"Ambry Genetics"[submitter] AND "RNASEH2B-AS1"[gene] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1467438	NM_024570.4(RNASEH2B):c.29G>A (p.Gly10Glu)	LOC130009810, RNASEH2B +1 more (G10E)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance
Select item 1027230	NM_024570.4(RNASEH2B):c.52T>A (p.Phe18Ile)	RNASEH2B-AS1, LOC130009810 +1 more (F18I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GUncertain significance