List of variants in gene ADGRV1 reported as uncertain significance 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: 23

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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.14761G>A (p.Ala4921Thr)	rs200115167	0.00060
NM_032119.4(ADGRV1):c.1837C>A (p.Gln613Lys)	rs199587998	0.00059
NM_032119.4(ADGRV1):c.1849G>A (p.Val617Met)	rs199988872	0.00046
NM_032119.4(ADGRV1):c.5295C>G (p.Phe1765Leu)	rs201388114	0.00035
NM_032119.4(ADGRV1):c.596G>T (p.Ser199Ile)	rs61745496	0.00031
NM_032119.4(ADGRV1):c.7468G>A (p.Ala2490Thr)	rs143632883	0.00025
NM_032119.4(ADGRV1):c.12982G>A (p.Glu4328Lys)	rs182452385	0.00022
NM_032119.4(ADGRV1):c.6994A>T (p.Ile2332Phe)	rs193030567	0.00019
NM_032119.4(ADGRV1):c.13382A>G (p.His4461Arg)	rs182698253	0.00017
NM_032119.4(ADGRV1):c.18754G>A (p.Asp6252Asn)	rs201800819	0.00016
NM_032119.4(ADGRV1):c.10768A>T (p.Ser3590Cys)	rs183319660	0.00010
NM_032119.4(ADGRV1):c.1684G>T (p.Ala562Ser)	rs199636312	0.00006
NM_032119.4(ADGRV1):c.1094A>G (p.Asp365Gly)	rs779719772	0.00003
NM_032119.4(ADGRV1):c.10882C>T (p.Pro3628Ser)	rs564470089	0.00001
NM_032119.4(ADGRV1):c.17276A>G (p.Asn5759Ser)	rs375445058	0.00001
NM_032119.4(ADGRV1):c.323C>G (p.Pro108Arg)	rs1158908533	0.00001
NM_032119.4(ADGRV1):c.5707T>A (p.Trp1903Arg)	rs1554081484	0.00001
NM_032119.4(ADGRV1):c.690A>C (p.Glu230Asp)	rs397517434	0.00001
NM_032119.4(ADGRV1):c.1364T>G (p.Val455Gly)	rs1580510493
NM_032119.4(ADGRV1):c.17683G>A (p.Val5895Ile)	rs1025278736
NM_032119.4(ADGRV1):c.18674G>T (p.Ser6225Ile)	rs1796208718
NM_032119.4(ADGRV1):c.7150C>T (p.Arg2384Trp)	rs377475657

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