List of variants in gene NUBPL reported as likely benign 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_025152.3(NUBPL):c.*537dup	rs200626091	0.09955
NM_025152.3(NUBPL):c.*1451C>T	rs28533800	0.03631
NM_025152.3(NUBPL):c.*26C>G	rs76130953	0.01425
NM_025152.3(NUBPL):c.593A>C (p.Asn198Thr)	rs11558436	0.00480

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