ClinVar Miner

List of variants in gene ADGRV1 reported as uncertain significance by GeneDx

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Total variants: 19
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HGVS dbSNP
GRCh38/hg38 5q14.3(chr5:90590733-90849185)x3
NM_032119.4(ADGRV1):c.10411_10412delinsAG (p.Glu3471Arg) rs1131691886
NM_032119.4(ADGRV1):c.1051A>G (p.Ile351Val) rs754152833
NM_032119.4(ADGRV1):c.10796G>C (p.Gly3599Ala) rs145294917
NM_032119.4(ADGRV1):c.11201T>C (p.Val3734Ala) rs113498662
NM_032119.4(ADGRV1):c.11549A>G (p.Lys3850Arg) rs1057524659
NM_032119.4(ADGRV1):c.11974G>A (p.Asp3992Asn) rs201386977
NM_032119.4(ADGRV1):c.12349C>T (p.Arg4117Cys) rs138908576
NM_032119.4(ADGRV1):c.12542C>T (p.Pro4181Leu) rs200957385
NM_032119.4(ADGRV1):c.13228G>A (p.Glu4410Lys) rs371970388
NM_032119.4(ADGRV1):c.13358A>G (p.His4453Arg) rs200212083
NM_032119.4(ADGRV1):c.13996A>G (p.Ile4666Val) rs765672841
NM_032119.4(ADGRV1):c.18746T>G (p.Leu6249Arg) rs41311625
NM_032119.4(ADGRV1):c.3116C>T (p.Ala1039Val) rs1338827370
NM_032119.4(ADGRV1):c.6317C>T (p.Ala2106Val) rs186999408
NM_032119.4(ADGRV1):c.8266G>A (p.Gly2756Arg) rs546198768
NM_032119.4(ADGRV1):c.8779G>A (p.Val2927Ile) rs547397177
NM_032119.4(ADGRV1):c.8815C>T (p.Pro2939Ser) rs202211640
NM_032119.4(ADGRV1):c.9661G>A (p.Val3221Met) rs368092861

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