List of variants in gene combination GSK3A, LOC130064563 reported as uncertain significance for muscle tissue disorder

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: 1

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HGVS	dbSNP	gnomAD frequency
NM_019884.3(GSK3A):c.146G>C (p.Gly49Ala)	rs1131690798

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