List of variants reported as risk factor for central nervous system neoplasm

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_000059.4(BRCA2):c.5645C>G (p.Ser1882Ter)	rs80358785
NM_000059.4(BRCA2):c.658_659del (p.Val220fs)	rs80359604
NM_003079.5(SMARCE1):c.237+2T>C	rs397509406
NM_003079.5(SMARCE1):c.311G>A (p.Trp104Ter)	rs397509407
NM_003079.5(SMARCE1):c.572dup (p.Ala192fs)	rs397509408
NM_003079.5(SMARCE1):c.715C>T (p.Arg239Ter)	rs397509405
NM_016169.4(SUFU):c.367C>T (p.Arg123Cys)	rs202247756
NM_032489.3(ACRBP):c.1040dup (p.Tyr348fs)	rs1949067963

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.