Variants in gene combination FANCD2, LOC107303338 with conflicting interpretations reported as "uncertain significance and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001018115.3(FANCD2):c.311T>C (p.Ile104Thr)	rs143936557	0.00115
NM_001018115.3(FANCD2):c.986C>G (p.Ala329Gly)	rs116736407	0.00113
NM_001018115.3(FANCD2):c.78A>C (p.Gln26His)	rs45510294	0.00075
NM_001018115.3(FANCD2):c.1777C>T (p.Pro593Ser)	rs147523071	0.00071
NM_001018115.3(FANCD2):c.182C>T (p.Thr61Met)	rs35110529	0.00045
NM_001018115.3(FANCD2):c.2273G>C (p.Cys758Ser)	rs540805431	0.00037
NM_001018115.3(FANCD2):c.2180C>T (p.Pro727Leu)	rs146509445	0.00036
NM_001018115.3(FANCD2):c.1118C>T (p.Ser373Leu)	rs372534421	0.00016
NM_001018115.3(FANCD2):c.1348A>G (p.Ile450Val)	rs145129959	0.00016
NM_001018115.3(FANCD2):c.672C>T (p.His224=)	rs371928644	0.00008
NM_001018115.3(FANCD2):c.1338A>C (p.Leu446=)	rs752268889	0.00007
NM_001018115.3(FANCD2):c.2004C>G (p.Ser668=)	rs138189144	0.00001
NM_001018115.3(FANCD2):c.2022-5C>T	rs4019784
NM_001018115.3(FANCD2):c.2613A>C (p.Lys871Asn)	rs56041034

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.