ClinVar Miner

Submissions for variant NM_001300.6(KLF6):c.*46A>T

dbSNP: rs483352821
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
Centre for molecular medicine, Karolinska Institutet RCV000119252 SCV000154104 not provided Hypotension no assertion provided not provided

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