List of variants in gene combination CRPPA, LOC129389757 reported as likely benign for hereditary skeletal muscle disorder

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_001101426.4(CRPPA):c.1264C>T (p.Leu422=)	rs375514450	0.00003
NM_001101426.4(CRPPA):c.1252-19G>T
NM_001101426.4(CRPPA):c.1257T>C (p.Asp419=)	rs2128361098
NM_001101426.4(CRPPA):c.1263G>A (p.Lys421=)
NM_001101426.4(CRPPA):c.1269G>A (p.Gln423=)

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