List of variants in gene LAMA3 reported as likely benign by Illumina Laboratory Services, Illumina

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.7797C>T (p.Asp2599=)	rs61751706	0.00523
NM_198129.4(LAMA3):c.6805C>G (p.Leu2269Val)	rs138591939	0.00303
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.7218C>T (p.Asp2406=)	rs62093184	0.00134
NM_198129.4(LAMA3):c.6436G>A (p.Ala2146Thr)	rs146005577	0.00023
NM_198129.4(LAMA3):c.7928G>T (p.Arg2643Leu)	rs45516998
NM_198129.4(LAMA3):c.8576+7G>T	rs1258107

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