ClinVar Miner

List of variants in gene RPS19 reported as uncertain significance by PreventionGenetics, part of Exact Sciences

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001022.4(RPS19):c.227C>T (p.Thr76Ile)	rs1356155484	0.00003
NM_001022.4(RPS19):c.173-9T>C	rs782552614	0.00001

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