ClinVar Miner

List of variants in gene combination AQP2, LOC101927318 reported as 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.*1562T>C rs296766
NM_000486.5(AQP2):c.*1684T>C rs10875989
NM_000486.5(AQP2):c.*1757A>G rs74091162
NM_000486.5(AQP2):c.*2292_*2295delCTCT rs72283122
NM_000486.5(AQP2):c.*2495A>G rs296768
NM_000486.5(AQP2):c.*2725A>C rs1077520
NM_000486.5(AQP2):c.*3002G>C rs2878771
NM_000486.5(AQP2):c.*3168T>C rs2878772
NM_000486.5(AQP2):c.*374C>T rs467323

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