List of variants in gene RNF41 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_005785.4(RNF41):c.277G>A (p.Val93Ile)	rs142114673	0.00030
NM_005785.4(RNF41):c.16A>G (p.Thr6Ala)	rs150381609	0.00016
NM_005785.4(RNF41):c.353A>G (p.Gln118Arg)	rs778144429	0.00007
NM_005785.4(RNF41):c.733G>A (p.Glu245Lys)	rs753102644	0.00001
NM_005785.4(RNF41):c.31G>A (p.Asp11Asn)
NM_005785.4(RNF41):c.416G>A (p.Arg139His)
NM_005785.4(RNF41):c.464C>T (p.Thr155Met)
NM_005785.4(RNF41):c.582T>G (p.Ile194Met)	rs1232893953
NM_005785.4(RNF41):c.718G>C (p.Ala240Pro)	rs1265909484
NM_005785.4(RNF41):c.808C>T (p.Arg270Cys)
NM_005785.4(RNF41):c.826G>C (p.Val276Leu)
NM_005785.4(RNF41):c.94C>T (p.Pro32Ser)	rs138861137

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