List of variants in gene ZNF772 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_001144068.2(ZNF772):c.287G>T (p.Gly96Val)	rs149559142	0.00556
NM_001144068.2(ZNF772):c.1225G>A (p.Val409Ile)	rs758330388	0.00001
NM_001144068.2(ZNF772):c.199+526T>C	rs2514430508
NM_001144068.2(ZNF772):c.487A>G (p.Lys163Glu)
NM_001144068.2(ZNF772):c.653C>T (p.Ser218Phe)

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