List of variants in gene TMEM216 reported as benign for Meckel syndrome

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: 7

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_001173990.3(TMEM216):c.264G>A (p.Pro88=)	rs3741265	0.84043
NM_001173990.3(TMEM216):c.432-11_432-10insA	rs11382548	0.83974
NM_001173990.3(TMEM216):c.*558G>A	rs7607	0.73129
NM_001173990.3(TMEM216):c.-2G>T	rs7107543	0.08005
NM_001173990.3(TMEM216):c.35-17C>T	rs147953784	0.00450
NM_001173990.3(TMEM216):c.432-1G>C	rs10897158
NM_001173990.3:c.432-11_432-10insA

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.