List of variants in gene RNASEH1 reported as likely benign by GeneDx

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 16

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HGVS	dbSNP	gnomAD frequency
NM_002936.6(RNASEH1):c.509+238G>A	rs114645635	0.03576
NM_002936.6(RNASEH1):c.129-94A>G	rs112137627	0.00723
NM_002936.6(RNASEH1):c.702A>G (p.Ala234=)	rs143510329	0.00685
NM_002936.6(RNASEH1):c.128+221C>T	rs148132213	0.00625
NM_002936.6(RNASEH1):c.774+190G>T	rs183665731	0.00483
NM_002936.6(RNASEH1):c.775-152G>A	rs115373330	0.00398
NM_002936.6(RNASEH1):c.244+334C>T	rs377310356	0.00397
NM_002936.6(RNASEH1):c.410-121G>A	rs138593515	0.00288
NM_002936.6(RNASEH1):c.474A>G (p.Ala158=)	rs61738918	0.00110
NM_002936.6(RNASEH1):c.720C>T (p.Asn240=)	rs140187158	0.00041
NM_002936.6(RNASEH1):c.441C>T (p.Cys147=)	rs769813042	0.00024
NM_002936.6(RNASEH1):c.156G>A (p.Arg52=)	rs148031856	0.00015
NM_002936.6(RNASEH1):c.417C>T (p.Phe139=)	rs139176330	0.00015
NM_002936.6(RNASEH1):c.569C>T (p.Ala190Val)	rs200811242	0.00008
NM_002936.6(RNASEH1):c.245-209_245-190del	rs1558456573
NM_002936.6(RNASEH1):c.509+206_509+207dup	rs1162099553

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