List of variants in gene RNF41 reported as benign by Breakthrough Genomics, Breakthrough Genomics

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_005785.4(RNF41):c.499-206C>A	rs773663	0.87831
NM_005785.4(RNF41):c.602+193T>C	rs703823	0.84206
NM_005785.4(RNF41):c.-23-73G>A	rs4759218	0.78363
NM_005785.4(RNF41):c.91-137A>G	rs7962107	0.03962
NM_005785.4(RNF41):c.447C>T (p.Ile149=)	rs17118378	0.01041
NM_005785.4(RNF41):c.91-121G>A	rs7975405

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