Variants in gene LAMA1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 10

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HGVS	dbSNP	gnomAD frequency
NM_005559.4(LAMA1):c.5302G>A (p.Val1768Met)	rs73938527	0.00297
NM_005559.4(LAMA1):c.2657C>T (p.Ala886Val)	rs144738522	0.00225
NM_005559.4(LAMA1):c.6354C>T (p.Val2118=)	rs150849018	0.00180
NM_005559.4(LAMA1):c.2900G>A (p.Gly967Asp)	rs141851670	0.00148
NM_005559.4(LAMA1):c.5867A>G (p.Asn1956Ser)	rs117433399	0.00137
NM_005559.4(LAMA1):c.8447G>A (p.Arg2816Gln)	rs200996196	0.00031
NM_005559.4(LAMA1):c.4066G>A (p.Ala1356Thr)	rs141657203	0.00021
NM_005559.4(LAMA1):c.8315G>A (p.Arg2772His)	rs548903685	0.00015
NM_005559.4(LAMA1):c.3256G>A (p.Asp1086Asn)	rs201831309	0.00010
NM_005559.4(LAMA1):c.4618G>A (p.Asp1540Asn)	rs373453681	0.00004

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