List of variants in gene CTAGE15 reported as likely benign

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001008747.2(CTAGE15):c.1261G>A (p.Glu421Lys)
NM_001008747.2(CTAGE15):c.1409G>A (p.Arg470Gln)	rs534347775
NM_001008747.2(CTAGE15):c.1555G>T (p.Ala519Ser)	rs768865277

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