List of variants in gene LAMA4 reported as benign by Genome Diagnostics Laboratory, University Medical Center Utrecht

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_001105206.3(LAMA4):c.460C>T (p.Arg154Trp)	rs11757455	0.04245
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.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.422+20G>T	rs188820838	0.00271
NM_001105206.3(LAMA4):c.5450T>C (p.Ile1817Thr)	rs144482486	0.00228
NM_001105206.3(LAMA4):c.5207-14G>C	rs112265545	0.00214
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.2250G>A (p.Gln750=)	rs112305543	0.00180

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