List of variants in gene CCDC39 reported as uncertain significance by Fulgent Genetics, Fulgent Genetics

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_181426.2(CCDC39):c.2057A>G (p.Asn686Ser)	rs201586263	0.00032
NM_181426.2(CCDC39):c.1885C>T (p.Arg629Cys)	rs199526690	0.00016
NM_181426.2(CCDC39):c.137G>A (p.Arg46His)	rs376716008	0.00004
NM_181426.2(CCDC39):c.2T>C (p.Met1Thr)	rs758493174	0.00004
NM_181426.2(CCDC39):c.531A>G (p.Gln177=)	rs779897284	0.00001
NM_181426.2(CCDC39):c.1359C>A (p.Ser453Arg)	rs6769457
NM_181426.2(CCDC39):c.64GAG[1] (p.Glu23del)	rs771715698

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