ClinVar Miner

Submissions for variant NM_001256643.1(LTA4H):c.88-6908C>T

gnomAD frequency: 0.00036  dbSNP: rs281860641
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
Functional Genomics, Thrombosis Research Institute, India RCV000106292 SCV000143749 not provided not provided no assertion provided not provided

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