List of variants in gene LAMA2 reported as benign by Athena Diagnostics Inc

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: 27

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HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.381C>A (p.Thr127=)	rs4404787	0.95273
NM_000426.4(LAMA2):c.7830G>C (p.Val2610=)	rs2229849	0.63028
NM_000426.4(LAMA2):c.5466A>G (p.Glu1822=)	rs3749877	0.50817
NM_000426.4(LAMA2):c.7760= (p.Ala2587=)	rs2229848	0.37054
NM_000426.4(LAMA2):c.2799A>G (p.Gln933=)	rs1027199	0.26612
NM_000426.4(LAMA2):c.1856G>A (p.Arg619His)	rs3816665	0.25723
NM_000426.4(LAMA2):c.156C>T (p.Ile52=)	rs1140366	0.08370
NM_000426.4(LAMA2):c.4956C>G (p.Thr1652=)	rs17057184	0.07998
NM_000426.4(LAMA2):c.6274+4C>T	rs73775410	0.02805
NM_000426.4(LAMA2):c.8028T>C (p.Asn2676=)	rs35313209	0.02285
NM_000426.4(LAMA2):c.8528A>G (p.Asn2843Ser)	rs73599293	0.02196
NM_000426.4(LAMA2):c.7431A>T (p.Arg2477Ser)	rs34367843	0.00914
NM_000426.4(LAMA2):c.8548-10T>C	rs113644365	0.00865
NM_000426.4(LAMA2):c.9123C>T (p.Val3041=)	rs61749497	0.00858
NM_000426.4(LAMA2):c.1403C>G (p.Ala468Gly)	rs111695726	0.00720
NM_000426.4(LAMA2):c.4437-5T>A	rs41285288	0.00557
NM_000426.4(LAMA2):c.4470C>T (p.Asp1490=)	rs35089085	0.00547
NM_000426.4(LAMA2):c.4487C>T (p.Ala1496Val)	rs147077184	0.00338
NM_000426.4(LAMA2):c.5909G>C (p.Cys1970Ser)	rs148451013	0.00314
NM_000426.4(LAMA2):c.4935C>A (p.Thr1645=)	rs35579821	0.00306
NM_000426.4(LAMA2):c.675C>T (p.Ala225=)	rs139665175	0.00298
NM_000426.4(LAMA2):c.5247C>T (p.Ala1749=)	rs149951387	0.00271
NM_000426.4(LAMA2):c.6429+8C>A	rs199773264	0.00238
NM_000426.4(LAMA2):c.411G>A (p.Ala137=)	rs149347601	0.00206
NM_000426.4(LAMA2):c.2430A>C (p.Pro810=)	rs147572139	0.00185
NM_000426.4(LAMA2):c.1586G>A (p.Ser529Asn)	rs370691060	0.00005
NM_000426.4(LAMA2):c.5072-6del	rs398123376

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