List of variants in gene RNASEH2A studied for not specified

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_006397.3(RNASEH2A):c.127+72T>C	rs13345720	0.11980
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.777C>T (p.Ser259=)	rs76634951	0.02171
NM_006397.3(RNASEH2A):c.615T>A (p.Asp205Glu)	rs62619782	0.01693
NM_006397.3(RNASEH2A):c.684C>T (p.Phe228=)	rs147131347	0.00078
NM_006397.3(RNASEH2A):c.662A>G (p.Lys221Arg)	rs143534021	0.00048
NM_006397.3(RNASEH2A):c.746C>T (p.Ala249Val)	rs758719669	0.00009
NM_006397.3(RNASEH2A):c.719C>T (p.Thr240Met)	rs79843600	0.00003
NM_006397.3(RNASEH2A):c.703C>T (p.Arg235Trp)	rs773112247	0.00002
NM_006397.3(RNASEH2A):c.411+3G>C	rs749477709	0.00001
NM_006397.3(RNASEH2A):c.322C>G (p.Arg108Gly)	rs76436818
NM_006397.3(RNASEH2A):c.635A>T (p.Asn212Ile)	rs377244188

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