List of variants in gene combination ZNF69, ZNF763 reported as likely benign for not specified

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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_001367172.2(ZNF763):c.569G>A (p.Arg190His)	rs370964246	0.00005
NM_001367172.2(ZNF763):c.731G>A (p.Arg244Gln)	rs376999343	0.00004
NM_001367172.2(ZNF763):c.121A>G (p.Thr41Ala)	rs757698014
NM_001367172.2(ZNF763):c.17G>T (p.Cys6Phe)	rs200170833
NM_001367172.2(ZNF763):c.882T>G (p.Ser294Arg)

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