List of variants in gene PAX7 reported as uncertain significance for hereditary skeletal muscle 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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001135254.2(PAX7):c.644G>A (p.Arg215His)	rs200575057	0.00047
NM_001135254.2(PAX7):c.1402+91T>G	rs2089708295
NM_001135254.2(PAX7):c.398T>C (p.Ile133Thr)	rs1427053032
NM_001135254.2(PAX7):c.739C>T (p.Arg247Cys)

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