ClinVar Miner

Variants in gene ADGRV1 with conflicting interpretations "benign" and "uncertain significance"

Submission 1 (benign) minimum review status: Submission 1 (benign) method:
Submission 2 (uncertain significance) minimum review status: Submission 2 (uncertain significance) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 20
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HGVS dbSNP
NM_032119.4(ADGRV1):c.10149C>T (p.Ser3383=) rs376298949
NM_032119.4(ADGRV1):c.10563T>C (p.Leu3521=) rs200946170
NM_032119.4(ADGRV1):c.10796G>C (p.Gly3599Ala) rs145294917
NM_032119.4(ADGRV1):c.1522A>C (p.Ile508Leu) rs61744480
NM_032119.4(ADGRV1):c.15608A>G (p.Glu5203Gly) rs202106463
NM_032119.4(ADGRV1):c.15786C>T (p.Phe5262=) rs369083434
NM_032119.4(ADGRV1):c.16377G>T (p.Gln5459His) rs371947306
NM_032119.4(ADGRV1):c.1776C>A (p.Val592=) rs184127858
NM_032119.4(ADGRV1):c.1849G>A (p.Val617Met) rs199988872
NM_032119.4(ADGRV1):c.18746T>G (p.Leu6249Arg) rs41311625
NM_032119.4(ADGRV1):c.2112G>A (p.Pro704=) rs182990046
NM_032119.4(ADGRV1):c.2261T>C (p.Val754Ala) rs374609813
NM_032119.4(ADGRV1):c.4214C>T (p.Ser1405Phe) rs41305898
NM_032119.4(ADGRV1):c.5830G>A (p.Asp1944Asn) rs41302834
NM_032119.4(ADGRV1):c.6133G>A (p.Gly2045Arg) rs41308846
NM_032119.4(ADGRV1):c.6317C>T (p.Ala2106Val) rs186999408
NM_032119.4(ADGRV1):c.6559A>G (p.Ile2187Val) rs200512504
NM_032119.4(ADGRV1):c.6994A>T (p.Ile2332Phe) rs193030567
NM_032119.4(ADGRV1):c.8730+9_8730+10del rs780180737
NM_032119.4(ADGRV1):c.9213C>T (p.Asp3071=) rs56329646

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