List of variants in gene ADGRV1 reported as uncertain significance by Joint Genome Diagnostic Labs from Nijmegen and Maastricht, Radboudumc and MUMC+

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: 7

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.11974G>A (p.Asp3992Asn)	rs201386977	0.00131
NM_032119.4(ADGRV1):c.1849G>A (p.Val617Met)	rs199988872	0.00046
NM_032119.4(ADGRV1):c.853C>G (p.Arg285Gly)	rs200197273	0.00046
NM_032119.4(ADGRV1):c.1718G>T (p.Gly573Val)	rs200789563	0.00036
NM_032119.4(ADGRV1):c.7867G>A (p.Glu2623Lys)	rs146526977	0.00019
NM_032119.4(ADGRV1):c.2636C>T (p.Thr879Met)	rs201007778	0.00014
NM_032119.4(ADGRV1):c.4108T>G (p.Phe1370Val)	rs1561464218

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