List of variants in gene combination LAMA3, LOC126862707 reported as uncertain significance for Laryngo-onycho-cutaneous syndrome

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_000227.6(LAMA3):c.30C>T (p.Cys10=)	rs145044428	0.00090
NM_000227.6(LAMA3):c.128A>C (p.Gln43Pro)	rs760019923	0.00005
NM_000227.6(LAMA3):c.71A>G (p.Gln24Arg)	rs1349909774	0.00002
NM_000227.6(LAMA3):c.19C>T (p.Arg7Trp)	rs139495056

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