ClinVar Miner

List of variants in gene TTC8 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (902):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 6
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HGVS dbSNP
NM_144596.3(TTC8):c.*472A>C rs59300815
NM_144596.3(TTC8):c.1077C>T (p.Asn359=) rs150896551
NM_144596.3(TTC8):c.1432-12T>C rs79747892
NM_144596.3(TTC8):c.357T>C (p.Ile119=) rs567203939
NM_144596.3(TTC8):c.528T>C (p.Asn176=) rs1555391010
NM_144596.3(TTC8):c.642C>G (p.Ala214=) rs141305911

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