List of variants in gene RPS19 reported as uncertain significance by Ambry 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_001022.4(RPS19):c.411+16G>C	rs782664193	0.00002
NM_001022.4(RPS19):c.109G>T (p.Val37Phe)	rs781861716
NM_001022.4(RPS19):c.112A>C (p.Lys38Gln)	rs138395296
NM_001022.4(RPS19):c.320T>C (p.Leu107Pro)	rs2513683341
NM_001022.4(RPS19):c.368T>A (p.Leu123Gln)	rs2513684988
NM_001022.4(RPS19):c.72-9T>A	rs2513667055

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