List of variants in gene ADGRV1 reported as likely benign by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

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: 11

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.746G>A (p.Arg249Lys)	rs41303344	0.00668
NM_032119.4(ADGRV1):c.11201T>C (p.Val3734Ala)	rs113498662	0.00189
NM_032119.4(ADGRV1):c.5072C>T (p.Thr1691Met)	rs146954342	0.00145
NM_032119.4(ADGRV1):c.4214C>T (p.Ser1405Phe)	rs41305898	0.00104
NM_032119.4(ADGRV1):c.6559A>G (p.Ile2187Val)	rs200512504	0.00037
NM_032119.4(ADGRV1):c.2456G>A (p.Ser819Asn)	rs182395524	0.00014
NM_032119.4(ADGRV1):c.6684T>A (p.Ser2228=)	rs373667458	0.00007
NM_032119.4(ADGRV1):c.14157A>G (p.Leu4719=)	rs779582048	0.00002
NM_032119.4(ADGRV1):c.15285T>C (p.Thr5095=)	rs745990374	0.00001
NM_032119.4(ADGRV1):c.6274+20TTA[4]	rs771346895
NM_032119.4(ADGRV1):c.8805T>G (p.Thr2935=)	rs1561569406

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