List of variants in gene combination CD27, LOC130007243 reported as uncertain significance for immune system 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001242.5(CD27):c.685G>A (p.Ala229Thr)	rs144240256	0.00008
NM_001242.5(CD27):c.671G>A (p.Ser224Asn)	rs149579617	0.00001
NM_001242.5(CD27):c.659-6C>T
NM_001242.5(CD27):c.674C>T (p.Pro225Leu)
NM_001242.5(CD27):c.696T>G (p.Cys232Trp)

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