ClinVar Miner

Submissions for variant NM_020458.4(TTC7A):c.666G>A (p.Thr222=)

gnomAD frequency: 0.00010  dbSNP: rs374954171
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV001520587 SCV001729720 benign Multiple gastrointestinal atresias 2021-11-18 criteria provided, single submitter clinical testing

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