List of variants in gene RBM15 reported as 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_022768.5(RBM15):c.2466T>C (p.Thr822=)	rs61745292	0.02349
NM_022768.5(RBM15):c.1617G>A (p.Gln539=)	rs61740988	0.00677
NM_022768.5(RBM15):c.486C>T (p.Gly162=)	rs60454212	0.00390

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