List of variants in gene LAMC3 reported as benign by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_006059.4(LAMC3):c.3244A>G (p.Ser1082Gly)	rs2275140	0.75621
NM_006059.4(LAMC3):c.219T>G (p.His73Gln)	rs3739512	0.56936
NM_006059.4(LAMC3):c.1932C>T (p.Ser644=)	rs12349966	0.48282
NM_006059.4(LAMC3):c.963C>T (p.Ala321=)	rs2275131	0.40359
NM_006059.4(LAMC3):c.4378-4A>G	rs4740413	0.38051
NM_006059.4(LAMC3):c.521C>A (p.Pro174His)	rs2275137	0.29468
NM_006059.4(LAMC3):c.4298C>T (p.Thr1433Met)	rs7024108	0.28739
NM_006059.4(LAMC3):c.1564C>T (p.Pro522Ser)	rs869457	0.28273
NM_006059.4(LAMC3):c.1218G>A (p.Thr406=)	rs2293518	0.20549
NM_006059.4(LAMC3):c.4477+13T>C	rs2275143	0.16247
NM_006059.4(LAMC3):c.454C>T (p.Arg152Cys)	rs45628035	0.00975
NM_006059.4(LAMC3):c.2308C>G (p.Arg770Gly)	rs3739510
NM_006059.4(LAMC3):c.855A>G (p.Ala285=)	rs2275132

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