List of variants in gene ADNP reported as benign by Ambry 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_001282531.3(ADNP):c.2568C>T (p.Val856=)	rs1062651	0.10055
NM_001282531.3(ADNP):c.2067C>T (p.Gly689=)	rs17790938	0.09265
NM_001282531.3(ADNP):c.2076G>A (p.Lys692=)	rs6096168	0.03400
NM_001282531.3(ADNP):c.1075A>G (p.Ile359Val)	rs78300927	0.00553
NM_001282531.3(ADNP):c.2475G>T (p.Gly825=)	rs148502910	0.00534
NM_001282531.3(ADNP):c.2666G>C (p.Ser889Thr)	rs34342624	0.00359
NM_001282531.3(ADNP):c.2743G>A (p.Val915Ile)	rs150900514	0.00236
NM_001282531.3(ADNP):c.909G>A (p.Met303Ile)	rs141172488	0.00050
NM_001282531.3(ADNP):c.191C>T (p.Thr64Met)	rs752399004	0.00001
NM_001282531.3(ADNP):c.2149C>T (p.Arg717Cys)
NM_001282531.3(ADNP):c.2809G>A (p.Glu937Lys)
NM_001282531.3(ADNP):c.833AGA[1] (p.Lys279del)	rs771131110

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