List of variants in gene ADGRV1 reported as pathogenic by CeGaT Center for Human Genetics Tuebingen

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.12895C>T (p.Arg4299Ter)	rs756954694	0.00001
NM_032119.4(ADGRV1):c.10935_10938del (p.Ser3646fs)	rs1754555183
NM_032119.4(ADGRV1):c.15916G>T (p.Gly5306Ter)
NM_032119.4(ADGRV1):c.1608C>A (p.Tyr536Ter)	rs1561416879
NM_032119.4(ADGRV1):c.16805del (p.Pro5602fs)	rs1765353894
NM_032119.4(ADGRV1):c.2790G>A (p.Trp930Ter)	rs1767488078

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