List of variants in gene RITA1 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_032848.3(RITA1):c.45C>T (p.Leu15=)	rs143269921	0.00007
NM_032848.3(RITA1):c.767G>A (p.Arg256Gln)	rs764901701	0.00001
NM_032848.3(RITA1):c.770G>A (p.Arg257Gln)	rs1458923693	0.00001
NM_032848.3(RITA1):c.553A>G (p.Met185Val)

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