List of variants in gene COL12A1 reported as benign for Bethlem myopathy 2

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_004370.6(COL12A1):c.5871T>A (p.Ala1957=)	rs594012	0.87959
NM_004370.6(COL12A1):c.9172G>A (p.Gly3058Ser)	rs970547	0.72620
NM_004370.6(COL12A1):c.7086+44C>G	rs499018	0.64687
NM_004370.6(COL12A1):c.5395-29G>A	rs1332020	0.42606
NM_004370.6(COL12A1):c.5213T>C (p.Ile1738Thr)	rs240736	0.28989
NM_004370.6(COL12A1):c.1892-19dup	rs11347601

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.