ClinVar Miner

List of variants in gene LAMA2 reported as benign by Illumina Clinical Services Laboratory,Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_000426.3(LAMA2):c.*193_*195delATA rs371188338
NM_000426.3(LAMA2):c.1856G>A (p.Arg619His) rs3816665
NM_000426.3(LAMA2):c.2799A>G (p.Gln933=) rs1027199
NM_000426.3(LAMA2):c.3411+13G>A rs3798663
NM_000426.3(LAMA2):c.381C>A (p.Thr127=) rs4404787
NM_000426.3(LAMA2):c.5466A>G (p.Glu1822=) rs3749877
NM_000426.3(LAMA2):c.5502G>A (p.Glu1834=) rs3749878
NM_000426.3(LAMA2):c.7830G>C (p.Val2610=) rs2229849
NM_000426.3(LAMA2):c.7845G>A (p.Pro2615=) rs2229850

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