List of variants in gene LAMA2 reported as uncertain significance by Genetic Services Laboratory, University of Chicago

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: 25

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HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.4487C>T (p.Ala1496Val)	rs147077184	0.00338
NM_000426.4(LAMA2):c.5633C>T (p.Ser1878Phe)	rs139586720	0.00279
NM_000426.4(LAMA2):c.1621A>G (p.Ser541Gly)	rs141363186	0.00175
NM_000426.4(LAMA2):c.2462C>T (p.Thr821Met)	rs117422805	0.00173
NM_000426.4(LAMA2):c.5021G>A (p.Arg1674Lys)	rs143333246	0.00090
NM_000426.4(LAMA2):c.922G>A (p.Glu308Lys)	rs146462599	0.00086
NM_000426.4(LAMA2):c.7415G>T (p.Gly2472Val)	rs200921233	0.00019
NM_000426.4(LAMA2):c.7088C>T (p.Thr2363Ile)	rs371403343	0.00017
NM_000426.4(LAMA2):c.5670G>T (p.Val1890=)	rs374587087	0.00009
NM_000426.4(LAMA2):c.8223G>A (p.Thr2741=)	rs150596964	0.00009
NM_000426.4(LAMA2):c.1369G>A (p.Ala457Thr)	rs542498391	0.00008
NM_000426.4(LAMA2):c.6274+5G>A	rs367765202	0.00006
NM_000426.4(LAMA2):c.8524A>G (p.Ile2842Val)	rs140178576	0.00006
NM_000426.4(LAMA2):c.6539A>T (p.Asp2180Val)	rs567385461	0.00004
NM_000426.4(LAMA2):c.9254G>A (p.Arg3085Gln)	rs776606476	0.00004
NM_000426.4(LAMA2):c.4471G>A (p.Asp1491Asn)	rs375640462	0.00003
NM_000426.4(LAMA2):c.1702A>G (p.Ser568Gly)	rs754994339	0.00002
NM_000426.4(LAMA2):c.3279C>T (p.Cys1093=)	rs371376404	0.00002
NM_000426.4(LAMA2):c.2122G>A (p.Ala708Thr)	rs777765933	0.00001
NM_000426.4(LAMA2):c.3110T>C (p.Ile1037Thr)	rs797045679	0.00001
NM_000426.4(LAMA2):c.4933A>G (p.Thr1645Ala)	rs1248916068	0.00001
NM_000426.4(LAMA2):c.5675A>T (p.Gln1892Leu)	rs779542581	0.00001
NM_000426.4(LAMA2):c.7369A>C (p.Asn2457His)	rs797045680	0.00001
NM_000426.4(LAMA2):c.-3A>G	rs764267708
NM_000426.4(LAMA2):c.4909G>C (p.Glu1637Gln)	rs138303386

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