List of variants in gene LAMA3 reported by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 23

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.4110G>A (p.Glu1370=)	rs112534534	0.00336
NM_198129.4(LAMA3):c.8629C>T (p.His2877Tyr)	rs35153125	0.00264
NM_198129.4(LAMA3):c.8028C>T (p.Asn2676=)	rs35737354	0.00238
NM_198129.4(LAMA3):c.4060G>A (p.Glu1354Lys)	rs34799994	0.00224
NM_198129.4(LAMA3):c.891G>A (p.Gly297=)	rs62093355	0.00223
NM_198129.4(LAMA3):c.4160G>A (p.Arg1387Gln)	rs112861599	0.00150
NM_198129.4(LAMA3):c.2809C>T (p.Leu937Phe)	rs61751701	0.00097
NM_198129.4(LAMA3):c.2919T>C (p.Asp973=)	rs376633949	0.00051
NM_198129.4(LAMA3):c.8069A>G (p.Gln2690Arg)	rs147208526	0.00042
NM_198129.4(LAMA3):c.4557C>T (p.Val1519=)	rs202215313	0.00040
NM_198129.4(LAMA3):c.1571G>A (p.Arg524His)	rs201845068	0.00031
NM_198129.4(LAMA3):c.6389C>T (p.Ser2130Phe)	rs199684626	0.00012
NM_198129.4(LAMA3):c.3171T>C (p.Tyr1057=)	rs142574930	0.00009
NM_198129.4(LAMA3):c.6567C>T (p.Ala2189=)	rs189589322	0.00006
NM_198129.4(LAMA3):c.8526G>A (p.Thr2842=)	rs546328935	0.00001
NM_198129.4(LAMA3):c.147G>A (p.Pro49=)
NM_198129.4(LAMA3):c.1812T>C (p.His604=)
NM_198129.4(LAMA3):c.1901A>G (p.His634Arg)
NM_198129.4(LAMA3):c.2206G>A (p.Gly736Ser)
NM_198129.4(LAMA3):c.2282A>T (p.Tyr761Phe)	rs1598856795
NM_198129.4(LAMA3):c.3932C>T (p.Pro1311Leu)
NM_198129.4(LAMA3):c.5047C>T (p.Arg1683Trp)
NM_198129.4(LAMA3):c.994C>T (p.Arg332Cys)

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