List of variants in gene RNASEH2C reported as uncertain significance by Women's Health and Genetics/Laboratory Corporation of America, LabCorp

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_032193.4(RNASEH2C):c.428A>G (p.Lys143Arg)
NM_032193.4(RNASEH2C):c.428A>T (p.Lys143Ile)	rs75146158
NM_032193.4(RNASEH2C):c.438_439dup (p.Ala147fs)	rs2495309013
NM_032193.4(RNASEH2C):c.469-7G>T	rs1857335838
NM_032193.4(RNASEH2C):c.495A>G (p.Ter165Trp)	rs749473518

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