List of variants studied for paragangliomas 4 by Counsyl

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total variants: 14

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_003000.3(SDHB):c.487T>C (p.Ser163Pro)	rs33927012	0.00921
NM_003000.3(SDHB):c.32G>A (p.Arg11His)	rs111430410	0.00185
NM_003000.3(SDHB):c.287-26A>G	rs201397253	0.00040
NM_003000.3(SDHB):c.642+17T>C	rs200597595	0.00016
NM_003000.3(SDHB):c.112C>T (p.Arg38Cys)	rs202119350	0.00006
NM_003000.3(SDHB):c.709C>T (p.Pro237Ser)	rs186768244	0.00004
NM_003000.3(SDHB):c.418G>T (p.Val140Phe)	rs267607032	0.00003
NM_003000.3(SDHB):c.352G>A (p.Asp118Asn)	rs200021702	0.00002
NM_003000.3(SDHB):c.765+13G>A	rs115561881	0.00002
NM_003000.3(SDHB):c.137G>A (p.Arg46Gln)	rs772551056	0.00001
NM_003000.3(SDHB):c.749C>T (p.Thr250Ile)	rs1057517537	0.00001
NM_003000.3(SDHB):c.287-1G>C	rs397516833
NM_003000.3(SDHB):c.424-14_424-9dup	rs1064794554
NM_003000.3(SDHB):c.79C>G (p.Arg27Gly)	rs74315369

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.