List of variants in gene CENPF reported as likely benign for Stromme syndrome

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_016343.4(CENPF):c.9081C>T (p.Leu3027=)	rs74557452	0.01439
NM_016343.4(CENPF):c.6214T>C (p.Ser2072Pro)	rs3748694	0.00004
NM_016343.4(CENPF):c.9200C>T (p.Thr3067Met)	rs752309258	0.00001

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