List of variants in gene ADCY10 reported as likely benign 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: 12

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HGVS	dbSNP	gnomAD frequency
NM_018417.6(ADCY10):c.3696C>T (p.His1232=)	rs61738852	0.01786
NM_018417.6(ADCY10):c.4377C>T (p.Tyr1459=)	rs61745244	0.00772
NM_018417.6(ADCY10):c.4752T>C (p.Ile1584=)	rs59725214	0.00762
NM_018417.6(ADCY10):c.3720T>C (p.Asn1240=)	rs61738760	0.00721
NM_018417.6(ADCY10):c.3765C>T (p.Tyr1255=)	rs148366922	0.00232
NM_018417.6(ADCY10):c.1902G>A (p.Val634=)	rs146639825	0.00081
NM_018417.6(ADCY10):c.2406G>A (p.Leu802=)	rs201086008	0.00035
NM_018417.6(ADCY10):c.3429T>C (p.Asn1143=)	rs149920420	0.00034
NM_018417.6(ADCY10):c.1742G>A (p.Arg581Gln)	rs377634034	0.00004
NM_018417.6(ADCY10):c.1668C>T (p.Thr556=)	rs200361556	0.00002
NM_018417.6(ADCY10):c.2308+11C>T	rs79898706
NM_018417.6(ADCY10):c.4815C>T (p.Thr1605=)	rs146952021

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