List of variants in gene LAMA4 reported as uncertain significance by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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_001105206.3(LAMA4):c.1541G>A (p.Arg514Gln)	rs146358872	0.00014
NM_001105206.3(LAMA4):c.1673C>T (p.Ala558Val)	rs137893207	0.00013
NM_001105206.3(LAMA4):c.3817T>C (p.Phe1273Leu)	rs781966924	0.00009
NM_001105206.3(LAMA4):c.964A>C (p.Lys322Gln)	rs1375382054	0.00003
NM_001105206.3(LAMA4):c.3506C>T (p.Pro1169Leu)	rs730880123	0.00002
NM_001105206.3(LAMA4):c.4111A>C (p.Ile1371Leu)	rs974775253	0.00001
NM_001105206.3(LAMA4):c.3708A>T (p.Arg1236Ser)	rs2114656750
NM_001105206.3(LAMA4):c.5135G>C (p.Gly1712Ala)	rs1777911531

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