List of variants in gene LAMA4 reported as benign 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: 21

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HGVS	dbSNP	gnomAD frequency
NM_001105206.3(LAMA4):c.423-4T>G	rs79008328	0.01927
NM_001105206.3(LAMA4):c.4173T>C (p.Tyr1391=)	rs35042032	0.01889
NM_001105206.3(LAMA4):c.280G>A (p.Gly94Ser)	rs35349917	0.01717
NM_001105206.3(LAMA4):c.196-12T>C	rs78871662	0.01634
NM_001105206.3(LAMA4):c.423-10C>T	rs75058449	0.01596
NM_001105206.3(LAMA4):c.4646A>G (p.Asn1549Ser)	rs12110554	0.01544
NM_001105206.3(LAMA4):c.531C>T (p.Pro177=)	rs61742228	0.01462
NM_001105206.3(LAMA4):c.195+144T>C	rs147118520	0.01345
NM_001105206.3(LAMA4):c.4065C>T (p.Phe1355=)	rs34753919	0.01154
NM_001105206.3(LAMA4):c.4287+15C>T	rs116361180	0.01137
NM_001105206.3(LAMA4):c.3239G>A (p.Arg1080Gln)	rs41289902	0.01045
NM_001105206.3(LAMA4):c.888C>T (p.Ser296=)	rs17073495	0.00461
NM_001105206.3(LAMA4):c.4314A>C (p.Ser1438=)	rs77367833	0.00251
NM_001105206.3(LAMA4):c.5016T>A (p.Ile1672=)	rs148517180	0.00210
NM_001105206.3(LAMA4):c.924T>C (p.His308=)	rs143580603	0.00205
NM_001105206.3(LAMA4):c.2493+15G>T	rs77901141	0.00178
NM_001105206.3(LAMA4):c.5443G>A (p.Val1815Ile)	rs3734292	0.00174
NM_001105206.3(LAMA4):c.1475T>A (p.Leu492His)	rs3752579	0.00093
NM_001105206.3(LAMA4):c.4678C>A (p.Arg1560=)	rs150069819	0.00078
NM_001105206.3(LAMA4):c.921T>G (p.Ala307=)	rs186498011	0.00045
NM_001105206.3(LAMA4):c.848_849= (p.Asp283=)	rs71543223

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