List of variants in gene LAMA4 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001105206.3(LAMA4):c.888C>T (p.Ser296=)	rs17073495	0.00461
NM_001105206.3(LAMA4):c.1614G>A (p.Ala538=)	rs143587921	0.00027
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val)	rs137893207	0.00013
NM_001105206.3(LAMA4):c.693C>T (p.Asp231=)	rs370231631	0.00004
NM_001105206.3(LAMA4):c.81G>C (p.Gly27=)

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