ClinVar Miner

List of variants in gene combination AQP2, LOC101927318 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (956):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_000486.5(AQP2):c.*1218T>C rs376984675
NM_000486.5(AQP2):c.*1228T>G rs77904078
NM_000486.5(AQP2):c.*1395C>T rs140054228
NM_000486.5(AQP2):c.*2101C>T rs77661963
NM_000486.5(AQP2):c.*2250C>T rs296767
NM_000486.5(AQP2):c.*252G>A rs114099597
NM_000486.5(AQP2):c.*2795T>G rs1077521
NM_000486.5(AQP2):c.*907C>T rs60887132
NM_000486.5(AQP2):c.438C>T (p.Phe146=) rs143886391

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