List of variants in gene LAMA2 reported as likely benign 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: 24

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HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.8028T>C (p.Asn2676=)	rs35313209	0.02285
NM_000426.4(LAMA2):c.8528A>G (p.Asn2843Ser)	rs73599293	0.02196
NM_000426.4(LAMA2):c.1533T>C (p.Asn511=)	rs9492266	0.02106
NM_000426.4(LAMA2):c.4750G>A (p.Gly1584Ser)	rs117781224	0.01941
NM_000426.4(LAMA2):c.1491T>C (p.Cys497=)	rs2306220	0.01733
NM_000426.4(LAMA2):c.8124T>A (p.Gly2708=)	rs34997144	0.01727
NM_000426.4(LAMA2):c.8691A>G (p.Arg2897=)	rs2228599	0.01648
NM_000426.4(LAMA2):c.3613A>G (p.Thr1205Ala)	rs35889149	0.01262
NM_000426.4(LAMA2):c.1798G>A (p.Gly600Arg)	rs36044314	0.01250
NM_000426.4(LAMA2):c.7431A>T (p.Arg2477Ser)	rs34367843	0.00914
NM_000426.4(LAMA2):c.1930C>G (p.His644Asp)	rs35879899	0.00899
NM_000426.4(LAMA2):c.8548-10T>C	rs113644365	0.00865
NM_000426.4(LAMA2):c.9123C>T (p.Val3041=)	rs61749497	0.00858
NM_000426.4(LAMA2):c.4935C>A (p.Thr1645=)	rs35579821	0.00306
NM_000426.4(LAMA2):c.6429+8C>A	rs199773264	0.00238
NM_000426.4(LAMA2):c.1308T>G (p.Gly436=)	rs41285286	0.00165
NM_000426.4(LAMA2):c.255C>T (p.Ile85=)	rs142083777	0.00116
NM_000426.4(LAMA2):c.2115T>G (p.Leu705=)	rs149753273	0.00065
NM_000426.4(LAMA2):c.7300+10T>A	rs200469923	0.00056
NM_000426.4(LAMA2):c.2217G>T (p.Trp739Cys)	rs192317605	0.00039
NM_000426.4(LAMA2):c.5382A>G (p.Thr1794=)	rs565429072	0.00003
NM_000426.4(LAMA2):c.3296A>G (p.Asn1099Ser)	rs35065563
NM_000426.4(LAMA2):c.3925-6T>A	rs372612467
NM_000426.4(LAMA2):c.5530C>A (p.Arg1844Ser)	rs56173620

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