List of variants in gene LAMA5 reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005560.6(LAMA5):c.2323+1G>A	rs370966549	0.00006
NM_005560.6(LAMA5):c.2171C>G (p.Ser724Cys)
NM_005560.6(LAMA5):c.5755G>C (p.Val1919Leu)

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