List of variants reported as uncertain significance for 3-M syndrome 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: 10

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014780.5(CUL7):c.2614G>A (p.Gly872Ser)	rs61750320	0.00170
NM_015311.3(OBSL1):c.75T>G (p.Ser25Arg)	rs376818200	0.00055
NM_014780.5(CUL7):c.2230G>A (p.Val744Met)	rs547138217	0.00011
NM_015311.3(OBSL1):c.3937G>A (p.Gly1313Arg)	rs766548555	0.00006
NM_014780.5(CUL7):c.587G>A (p.Arg196Gln)	rs761377936	0.00005
NM_015311.3(OBSL1):c.3292C>T (p.Arg1098Cys)	rs768636811	0.00004
NM_015311.3(OBSL1):c.3955C>T (p.Gln1319Ter)	rs1057518717	0.00002
NM_015311.3(OBSL1):c.3355C>T (p.Leu1119=)	rs750782462	0.00001
NM_032040.5(CCDC8):c.1094A>C (p.Asp365Ala)	rs141966158	0.00001
NM_015311.3(OBSL1):c.4005C>A (p.Asp1335Glu)	rs375716830

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.