ClinVar Miner

List of variants in gene RIT1 reported as likely benign for canthal anomaly

Included ClinVar conditions (57):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 11
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NM_006912.6(RIT1):c.106+10A>G rs781557110
NM_006912.6(RIT1):c.107-9C>G rs200597833
NM_006912.6(RIT1):c.131A>T (p.His44Leu)
NM_006912.6(RIT1):c.237+10C>A rs367785615
NM_006912.6(RIT1):c.313C>T (p.Arg105Cys)
NM_006912.6(RIT1):c.321T>C (p.Ser107=)
NM_006912.6(RIT1):c.393T>C (p.Leu131=) rs34974790
NM_006912.6(RIT1):c.498A>C (p.Ala166=)
NM_006912.6(RIT1):c.540G>A (p.Arg180=) rs369738767
NM_006912.6(RIT1):c.594G>A (p.Lys198=) rs779457410
NM_006912.6(RIT1):c.603C>T (p.Asn201=)

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