List of variants in gene RNF43 reported as benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_017763.6(RNF43):c.2261G>C (p.Gly754Ala)	rs115553539	0.00733
NM_017763.6(RNF43):c.380G>A (p.Arg127Gln)	rs35219874	0.00220
NM_017763.6(RNF43):c.1093G>A (p.Ala365Thr)	rs79309393	0.00135
NM_017763.6(RNF43):c.597G>A (p.Val199=)	rs77499318	0.00058
NM_017763.6(RNF43):c.2054C>A (p.Thr685Asn)	rs34464652	0.00038

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