List of variants in gene ZNF385C reported as uncertain significance for not specified

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_001392013.1(ZNF385C):c.520G>A (p.Glu174Lys)	rs1017608451	0.00011
NM_001392013.1(ZNF385C):c.1081C>T (p.Arg361Trp)	rs782302964	0.00009
NM_001392013.1(ZNF385C):c.1066A>G (p.Arg356Gly)	rs782361613	0.00001
NM_001392013.1(ZNF385C):c.562G>T (p.Ala188Ser)	rs2052734483

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