ClinVar Miner

List of variants in gene CLDN16 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (961):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 9
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HGVS dbSNP
NM_001378492.1(CLDN16):c.-93-158C>T
NM_006580.3(CLDN16):c.*1117G>A rs10470534
NM_006580.3(CLDN16):c.*1178C>T rs533709248
NM_006580.3(CLDN16):c.*907A>G rs116488781
NM_006580.3(CLDN16):c.166del (p.Ala56fs) rs368234054
NM_006580.3(CLDN16):c.836C>A (p.Ala279Asp)
NM_006580.4(CLDN16):c.*1812A>G
NM_006580.4(CLDN16):c.*181C>T
NM_006580.4(CLDN16):c.*1952C>G

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