List of variants in gene RNASEH2A reported as benign for autoinflammatory syndrome of childhood

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 13

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HGVS	dbSNP	gnomAD frequency
NM_006397.3(RNASEH2A):c.605T>C (p.Leu202Ser)	rs7247284	0.06918
NM_006397.3(RNASEH2A):c.550-11T>C	rs7247253	0.06913
NM_006397.3(RNASEH2A):c.462G>A (p.Gln154=)	rs7257575	0.06903
NM_006397.3(RNASEH2A):c.637+13G>A	rs73503453	0.05671
NM_006397.3(RNASEH2A):c.777C>T (p.Ser259=)	rs76634951	0.02157
NM_006397.3(RNASEH2A):c.615T>A (p.Asp205Glu)	rs62619782	0.01693
NM_006397.3(RNASEH2A):c.*120C>T	rs73925216	0.01285
NM_006397.3(RNASEH2A):c.412-6T>G	rs192358167	0.00277
NM_006397.3(RNASEH2A):c.339G>T (p.Leu113=)	rs145176499	0.00163
NM_006397.3(RNASEH2A):c.662A>G (p.Lys221Arg)	rs143534021	0.00038
NM_006397.3(RNASEH2A):c.411+17T>A	rs185730742	0.00031
NM_006397.3(RNASEH2A):c.549+10dup
NM_006397.3(RNASEH2A):c.550-9dup

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