List of variants in gene LAMA3 reported as 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_198129.4(LAMA3):c.8500= (p.Gly2834=)	rs1154233	0.99993
NM_198129.4(LAMA3):c.9352-7G>A	rs2241643	0.51794
NM_198129.4(LAMA3):c.*91C>T	rs1051150	0.51640
NM_198129.4(LAMA3):c.*89C>A	rs1051149	0.51636
NM_198129.4(LAMA3):c.6147C>G (p.Ala2049=)	rs1154226	0.21073
NM_198129.4(LAMA3):c.8445C>A (p.Asn2815Lys)	rs1154232	0.17201
NM_198129.4(LAMA3):c.8731C>T (p.Leu2911=)	rs1131521	0.15145
NM_198129.4(LAMA3):c.5322C>T (p.Phe1774=)	rs958631	0.08419
NM_198129.4(LAMA3):c.6555C>T (p.Ala2185=)	rs35872318	0.02513
NM_198129.4(LAMA3):c.*239G>A	rs45543834	0.01494
NM_198129.4(LAMA3):c.8104A>G (p.Thr2702Ala)	rs9952370	0.01207
NM_198129.4(LAMA3):c.9643-14C>T	rs72875942	0.00748
NM_198129.4(LAMA3):c.9353G>A (p.Ser3118Asn)	rs61749943	0.00618
NM_198129.4(LAMA3):c.*395A>T	rs138907590	0.00519
NM_198129.4(LAMA3):c.7818G>A (p.Thr2606=)	rs139567388	0.00426
NM_198129.4(LAMA3):c.6805C>G (p.Leu2269Val)	rs138591939	0.00303
NM_198129.4(LAMA3):c.9027-11G>A	rs117781425	0.00152
NM_198129.4(LAMA3):c.8898C>T (p.Ser2966=)	rs141164795	0.00121
NM_198129.4(LAMA3):c.8576+7G>C	rs1258107

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