List of variants reported as likely pathogenic for central nervous system neoplasm by Counsyl

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	gnomAD frequency
NM_004168.4(SDHA):c.1534C>T (p.Arg512Ter)	rs748089700	0.00005
NM_003000.3(SDHB):c.418G>T (p.Val140Phe)	rs267607032	0.00003
NM_003000.3(SDHB):c.137G>A (p.Arg46Gln)	rs772551056	0.00001
NM_004168.4(SDHA):c.1A>T (p.Met1Leu)	rs1061517
NM_004168.4(SDHA):c.210dup (p.Gly71fs)	rs1553997340
NM_004168.4(SDHA):c.2T>C (p.Met1Thr)	rs750380279
NM_004168.4(SDHA):c.757_758del (p.Val253fs)	rs1553998254

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.