List of variants in gene combination LOC130056175, POMT2 reported as likely benign for Muscular dystrophy-dystroglycanopathy (congenital with brain and eye anomalies), type A2; Muscular dystrophy-dystroglycanopathy (congenital with intellectual disability), type B2; Autosomal recessive limb-girdle muscular dystrophy type 2N

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: 4

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_013382.7(POMT2):c.672C>T (p.Pro224=)	rs147619625	0.00002
NM_013382.7(POMT2):c.660C>T (p.Pro220=)	rs1377744438	0.00001
NM_013382.7(POMT2):c.699C>T (p.Gly233=)	rs375257656	0.00001
NM_013382.7(POMT2):c.690C>T (p.Ser230=)	rs895876912

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.