"PreventionGenetics, part of Exact Sciences"[submitter] AND "RNASEH1"[ - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2195654	NM_002936.6(RNASEH1):c.852G>A (p.Ser284=)	RNASEH1	Single nucleotide variant (synonymous variant +2 more)	RNASEH1-related condition +1 more	GLikely benign
Select item 673568	NM_002936.6(RNASEH1):c.702A>G (p.Ala234=)	RNASEH1	Single nucleotide variant (synonymous variant +1 more)	RNASEH1-related condition +1 more	GBenign/Likely benign
Select item 2421338	NM_002936.6(RNASEH1):c.555G>A (p.Ala185=)	RNASEH1	Single nucleotide variant (synonymous variant +1 more)	RNASEH1-related condition +1 more	GLikely benign
Select item 1928720	NM_002936.6(RNASEH1):c.513T>C (p.Asn171=)	RNASEH1	Single nucleotide variant (synonymous variant +2 more)	RNASEH1-related condition +1 more	GLikely benign
Select item 730250	NM_002936.6(RNASEH1):c.474A>G (p.Ala158=)	RNASEH1	Single nucleotide variant (synonymous variant +1 more)	RNASEH1-related condition +1 more	GLikely benign
Select item 737361	NM_002936.6(RNASEH1):c.441C>T (p.Cys147=)	RNASEH1	Single nucleotide variant (synonymous variant +1 more)	RNASEH1-related condition +1 more	GLikely benign
Select item 739275	NM_002936.6(RNASEH1):c.411A>G (p.Gly137=)	RNASEH1	Single nucleotide variant (synonymous variant +2 more)	RNASEH1-related condition +1 more	GLikely benign
Select item 3008316	NM_002936.6(RNASEH1):c.396G>A (p.Thr132=)	RNASEH1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 2186868	NM_002936.6(RNASEH1):c.348G>A (p.Lys116=)	RNASEH1	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GLikely benign
Select item 2165276	NM_002936.6(RNASEH1):c.330C>T (p.Ser110=)	RNASEH1	Single nucleotide variant (synonymous variant +2 more)	not provided +1 more	GBenign/Likely benign
Select item 725826	NM_002936.6(RNASEH1):c.288C>T (p.Ser96=)	RNASEH1	Single nucleotide variant (synonymous variant +2 more)	RNASEH1-related condition +1 more	GBenign/Likely benign
Select item 2044139	NM_002936.6(RNASEH1):c.258A>G (p.Gln86=)	RNASEH1	Single nucleotide variant (synonymous variant +2 more)	RNASEH1-related condition +1 more	GBenign/Likely benign