List of variants reported as pathogenic for Mirage syndrome

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: 7

Download table as spreadsheet

HGVS	dbSNP
NM_017654.4(SAMD9):c.1376G>A (p.Arg459Gln)	rs1584254152
NM_017654.4(SAMD9):c.2305G>A (p.Asp769Asn)	rs1584253343
NM_017654.4(SAMD9):c.2920G>A (p.Glu974Lys)	rs1554336981
NM_017654.4(SAMD9):c.2944C>T (p.Arg982Cys)	rs0
NM_017654.4(SAMD9):c.2945G>A (p.Arg982His)	rs1554336974
NM_017654.4(SAMD9):c.3877C>T (p.Arg1293Trp)	rs1584251938
NM_017654.4(SAMD9):c.3878G>A (p.Arg1293Gln)	rs0

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.