List of variants in gene CD27 reported as likely benign by CeGaT Center for Human Genetics Tuebingen

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_001242.5(CD27):c.495C>T (p.Asp165=)	rs375150093	0.00014
NM_001242.5(CD27):c.714G>A (p.Arg238=)	rs770816422	0.00009
NM_001242.5(CD27):c.354C>T (p.Thr118=)	rs149051653	0.00001

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