List of variants in gene RTTN reported as likely benign by Fulgent Genetics, Fulgent Genetics

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_173630.4(RTTN):c.220-12T>C	rs11873759	0.02102
NM_173630.4(RTTN):c.32-3C>T	rs75577820	0.00750
NM_173630.4(RTTN):c.5745+13G>T	rs144392822	0.00745
NM_173630.4(RTTN):c.4889G>C (p.Arg1630Thr)	rs182595458	0.00389
NM_173630.4(RTTN):c.805T>C (p.Phe269Leu)	rs141156594	0.00096
NM_173630.4(RTTN):c.5319G>C (p.Ala1773=)	rs35439940

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