List of variants in gene RC3H1 reported as likely benign

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_172071.4(RC3H1):c.2137C>G (p.Gln713Glu)	rs77941945	0.00595
NM_172071.4(RC3H1):c.2116C>T (p.Pro706Ser)	rs143152120	0.00164
NM_172071.4(RC3H1):c.27G>A (p.Thr9=)	rs61742286	0.00046
NM_172071.4(RC3H1):c.1440A>G (p.Glu480=)

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