List of variants in gene LAMA3 reported as uncertain significance by Eurofins NTD LLC (GA)

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

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.8829G>A (p.Arg2943=)	rs141472847	0.00103
NM_198129.4(LAMA3):c.7505A>G (p.Asn2502Ser)	rs139823161	0.00029
NM_198129.4(LAMA3):c.6923C>A (p.Pro2308His)	rs886042515
NM_198129.4(LAMA3):c.7657C>G (p.Leu2553Val)	rs794727354

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