List of variants in gene LAMA2 reported by Genetics and Genomics Program, Sidra Medicine

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000426.4(LAMA2):c.8905C>T (p.Arg2969Cys)	rs374888837	0.00021
NM_000426.4(LAMA2):c.7057C>T (p.Arg2353Cys)	rs145885540	0.00016
NM_000426.4(LAMA2):c.8842G>A (p.Gly2948Ser)	rs143638361	0.00011
NM_000426.4(LAMA2):c.2735C>T (p.Ala912Val)	rs376580266	0.00003
NM_000426.4(LAMA2):c.4607C>T (p.Pro1536Leu)	rs1776956586
NM_000426.4(LAMA2):c.7040G>T (p.Gly2347Val)	rs529981007

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