ClinVar Miner

Submissions for variant NM_006440.5(TXNRD2):c.949+222C>T

gnomAD frequency: 0.00021  dbSNP: rs376616232
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
New York Genome Center RCV001255055 SCV001431146 uncertain significance not provided 2020-01-23 no assertion criteria provided clinical testing

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