List of variants in gene ADCY10 reported as likely benign by GeneDx

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_018417.6(ADCY10):c.3750+216C>T	rs114979527	0.03779
NM_018417.6(ADCY10):c.3418-155A>G	rs79602588	0.03157
NM_018417.6(ADCY10):c.3751-224T>C	rs79000836	0.02902
NM_018417.6(ADCY10):c.4058C>T (p.Pro1353Leu)	rs72697797	0.02736
NM_018417.6(ADCY10):c.2172-320T>C	rs76872780	0.01681
NM_018417.6(ADCY10):c.1810-21T>G	rs77906219	0.01297
NM_018417.6(ADCY10):c.2125A>G (p.Ile709Val)	rs112466731	0.00978
NM_018417.6(ADCY10):c.4313A>G (p.Asn1438Ser)	rs41270737	0.00817
NM_018417.6(ADCY10):c.3077+88T>C	rs76098951	0.00726
NM_018417.6(ADCY10):c.2309-166dup	rs148055144
NM_018417.6(ADCY10):c.3417+222_3417+225del	rs539820019
NM_018417.6(ADCY10):c.3417+224_3417+225del	rs539820019
NM_018417.6(ADCY10):c.4053-302del	rs34394385

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