List of variants in gene LAMA2 reported as benign by Eurofins NTD LLC (GA)

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: 37

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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.7760C>T (p.Ala2587Val)	rs2229848	0.62946
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.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.4523+19C>T	rs17057158	0.08168
NM_000426.4(LAMA2):c.4956C>G (p.Thr1652=)	rs17057184	0.07998
NM_000426.4(LAMA2):c.4750G>A (p.Gly1584Ser)	rs117781224	0.01941
NM_000426.4(LAMA2):c.8124T>A (p.Gly2708=)	rs34997144	0.01727
NM_000426.4(LAMA2):c.1798G>A (p.Gly600Arg)	rs36044314	0.01250
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.1701C>T (p.Ile567=)	rs111381107	0.00641
NM_000426.4(LAMA2):c.4437-5T>A	rs41285288	0.00557
NM_000426.4(LAMA2):c.2476C>T (p.Arg826Trp)	rs118147866	0.00549
NM_000426.4(LAMA2):c.4470C>T (p.Asp1490=)	rs35089085	0.00547
NM_000426.4(LAMA2):c.3556-15T>G	rs17741922	0.00414
NM_000426.4(LAMA2):c.1634T>A (p.Leu545Gln)	rs118083923	0.00359
NM_000426.4(LAMA2):c.8982T>C (p.Asp2994=)	rs79374915	0.00344
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.5633C>T (p.Ser1878Phe)	rs139586720	0.00279
NM_000426.4(LAMA2):c.5247C>T (p.Ala1749=)	rs149951387	0.00271
NM_000426.4(LAMA2):c.8755C>T (p.Pro2919Ser)	rs143026295	0.00224
NM_000426.4(LAMA2):c.6649G>A (p.Val2217Ile)	rs147857398	0.00093
NM_000426.4(LAMA2):c.5688C>T (p.His1896=)	rs573779258	0.00003
NM_000426.4(LAMA2):c.2756G>T (p.Arg919Leu)	rs35277491
NM_000426.4(LAMA2):c.3175-32_3175-31del	rs372962551
NM_000426.4(LAMA2):c.5072-6del	rs398123376
NM_000426.4(LAMA2):c.5530C>A (p.Arg1844Ser)	rs56173620

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