List of variants in gene combination CSTB, LOC130066788 reported as benign by GeneDx

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: 7

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HGVS	dbSNP	gnomAD frequency
NC_000021.9:g.43776481A>G	rs968436	0.99799
NM_000100.4(CSTB):c.66+89T>C	rs6369	0.23757
NM_000100.3(CSTB):c.-54C>T	rs59649299	0.03508
NM_000100.4(CSTB):c.15G>T (p.Ala5=)	rs4533	0.01694
NM_000100.4(CSTB):c.54C>T (p.His18=)	rs557717323	0.00073
NM_000100.3(CSTB):c.-42C>T	rs776181852	0.00016
NM_000100.2(CSTB):c.-36_-24delGAGTCCCCTCGCC	rs577227536

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