List of variants in gene RNF43 reported as benign by GeneDx

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: 17

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_017763.6(RNF43):c.1252C>A (p.Leu418Met)	rs2526374	0.37751
NM_017763.6(RNF43):c.139A>G (p.Ile47Val)	rs3744093	0.34578
NM_017763.6(RNF43):c.-385-51T>A	rs7215531	0.22893
NM_017763.6(RNF43):c.2309-15G>C	rs2158460	0.17956
NM_017763.6(RNF43):c.375+220T>C	rs2632513	0.15307
NM_017763.6(RNF43):c.582+110C>T	rs2526372	0.14625
NM_017763.6(RNF43):c.350G>A (p.Arg117His)	rs2257205	0.14132
NM_017763.6(RNF43):c.692C>T (p.Pro231Leu)	rs2680701	0.13626
NM_017763.6(RNF43):c.2057C>G (p.Pro686Arg)	rs9652855	0.11464
NM_017763.6(RNF43):c.1028G>A (p.Arg343His)	rs34523089	0.11188
NM_017763.6(RNF43):c.582+162C>T	rs2632517	0.06128
NM_017763.6(RNF43):c.849+102A>C	rs115746038	0.02551
NM_017763.6(RNF43):c.2309-29C>T	rs2158459	0.02153
NM_017763.6(RNF43):c.2261G>C (p.Gly754Ala)	rs115553539	0.00698
NM_017763.6(RNF43):c.582+30C>T	rs79125070	0.00260
NM_017763.6(RNF43):c.662G>A (p.Arg221Gln)	rs2285990	0.00161
NM_017763.6(RNF43):c.582+94C>A	rs2680700

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.