List of variants in gene RNASEH2B reported as likely pathogenic by Fulgent Genetics, Fulgent Genetics

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_024570.4(RNASEH2B):c.719C>G (p.Ser240Ter)	rs372632599	0.00002
NM_024570.4(RNASEH2B):c.136+1del	rs75186889
NM_024570.4(RNASEH2B):c.554T>G (p.Val185Gly)	rs74555752

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