List of variants in gene LAMA2 reported by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 12

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.8528A>G (p.Asn2843Ser)	rs73599293	0.02196
NM_000426.4(LAMA2):c.7431A>T (p.Arg2477Ser)	rs34367843	0.00914
NM_000426.4(LAMA2):c.4437-5T>A	rs41285288	0.00557
NM_000426.4(LAMA2):c.2476C>T (p.Arg826Trp)	rs118147866	0.00549
NM_000426.4(LAMA2):c.1634T>A (p.Leu545Gln)	rs118083923	0.00359
NM_000426.4(LAMA2):c.5909G>C (p.Cys1970Ser)	rs148451013	0.00314
NM_000426.4(LAMA2):c.74C>T (p.Pro25Leu)	rs145310035	0.00147
NM_000426.4(LAMA2):c.922G>A (p.Glu308Lys)	rs146462599	0.00086
NM_000426.4(LAMA2):c.8988+15T>C	rs201041465	0.00020
NM_000426.4(LAMA2):c.1303C>T (p.Arg435Ter)	rs773209126	0.00001
NM_000426.4(LAMA2):c.3296A>G (p.Asn1099Ser)	rs35065563
NM_000426.4(LAMA2):c.5530C>A (p.Arg1844Ser)	rs56173620

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.