List of variants in gene ADGRV1 reported as pathogenic by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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: 4

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HGVS	dbSNP	gnomAD frequency
NM_032119.4(ADGRV1):c.10458G>A (p.Trp3486Ter)	rs1580905929
NM_032119.4(ADGRV1):c.18883_18886del (p.Glu6295fs)	rs762597192
NM_032119.4(ADGRV1):c.6077dup (p.Tyr2026Ter)
NM_032119.4(ADGRV1):c.6856C>T (p.Arg2286Ter)	rs1746388061

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