List of variants in gene LAMA3 reported by Fulgent Genetics, Fulgent Genetics

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: 12

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.5942G>A (p.Arg1981Gln)	rs139393175	0.00017
NM_198129.4(LAMA3):c.8075G>A (p.Arg2692His)	rs139915002	0.00011
NM_198129.4(LAMA3):c.9027-14G>A	rs372927257	0.00010
NM_198129.4(LAMA3):c.6286A>G (p.Ile2096Val)	rs150757806	0.00008
NM_198129.4(LAMA3):c.4750C>T (p.Arg1584Ter)	rs552326056	0.00006
NM_198129.4(LAMA3):c.2332G>A (p.Gly778Arg)	rs367800328	0.00004
NM_198129.4(LAMA3):c.4297A>G (p.Thr1433Ala)	rs377141415	0.00004
NM_198129.4(LAMA3):c.6808C>T (p.Arg2270Ter)	rs137852757	0.00001
NM_198129.4(LAMA3):c.7158+1G>A	rs1057516279	0.00001
NM_198129.4(LAMA3):c.8941C>T (p.Gln2981Ter)	rs772038362	0.00001
NM_198129.4(LAMA3):c.734del (p.Phe245fs)	rs1555684238
NM_198129.4(LAMA3):c.856-2A>G	rs757101344

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