List of variants in gene LAMA3 reported as benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.2901T>C (p.Ala967=)	rs9962023	0.64176
NM_198129.4(LAMA3):c.9352-7G>A	rs2241643	0.51794
NM_198129.4(LAMA3):c.4260G>C (p.Gly1420=)	rs867449	0.48275
NM_198129.4(LAMA3):c.4530C>T (p.Pro1510=)	rs12965685	0.47260
NM_198129.4(LAMA3):c.6147C>G (p.Ala2049=)	rs1154226	0.21073
NM_198129.4(LAMA3):c.8445C>A (p.Asn2815Lys)	rs1154232	0.17201
NM_198129.4(LAMA3):c.8731C>T (p.Leu2911=)	rs1131521	0.15145
NM_198129.4(LAMA3):c.8576+7G>C	rs1258107

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