List of variants in gene LAMA2 reported as benign by Illumina Laboratory Services, Illumina

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: 29

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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.5502G>A (p.Glu1834=)	rs3749878	0.50693
NM_000426.4(LAMA2):c.7845G>A (p.Pro2615=)	rs2229850	0.35164
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.3411+13G>A	rs3798663	0.25503
NM_000426.4(LAMA2):c.*118T>C	rs1049476	0.25167
NM_000426.4(LAMA2):c.3412G>A (p.Val1138Met)	rs2306942	0.09135
NM_000426.4(LAMA2):c.7906A>G (p.Thr2636Ala)	rs2244008	0.08650
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.-72G>A	rs10080633	0.02533
NM_000426.4(LAMA2):c.8028T>C (p.Asn2676=)	rs35313209	0.02285
NM_000426.4(LAMA2):c.1533T>C (p.Asn511=)	rs9492266	0.02106
NM_000426.4(LAMA2):c.1491T>C (p.Cys497=)	rs2306220	0.01733
NM_000426.4(LAMA2):c.8124T>A (p.Gly2708=)	rs34997144	0.01727
NM_000426.4(LAMA2):c.8691A>G (p.Arg2897=)	rs2228599	0.01648
NM_000426.4(LAMA2):c.3613A>G (p.Thr1205Ala)	rs35889149	0.01262
NM_000426.4(LAMA2):c.*57A>C	rs1049473	0.01179
NM_000426.4(LAMA2):c.1206+11C>T	rs115007959	0.00915
NM_000426.4(LAMA2):c.1930C>G (p.His644Asp)	rs35879899	0.00899
NM_000426.4(LAMA2):c.2097-13T>C	rs139246515	0.00415
NM_000426.4(LAMA2):c.3556-15T>G	rs17741922	0.00414
NM_000426.4(LAMA2):c.*190ATA[1]	rs371188338
NM_000426.4(LAMA2):c.2756G>T (p.Arg919Leu)	rs35277491
NM_000426.4(LAMA2):c.9212-15C>A	rs55776770

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