List of variants reported as pathogenic for Amelogenesis imperfecta type 1G by Fulgent Genetics, Fulgent Genetics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 8

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_017565.4(FAM20A):c.406C>T (p.Arg136Ter)	rs144411158	0.00010
NM_017565.4(FAM20A):c.813-2A>G	rs587776912	0.00003
NM_017565.4(FAM20A):c.826C>T (p.Arg276Ter)	rs387907215	0.00001
NM_017565.4(FAM20A):c.1447del (p.Glu483fs)	rs762205955
NM_017565.4(FAM20A):c.466C>T (p.Arg156Ter)
NM_017565.4(FAM20A):c.727C>T (p.Arg243Ter)
NM_017565.4(FAM20A):c.907_908del (p.Ser303fs)
NM_017565.4(FAM20A):c.915_918del (p.Phe305fs)	rs760163489

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.