ClinVar Miner

Submissions for variant NM_001457.4(FLNB):c.602C>T (p.Ala201Val)

dbSNP: rs80356499
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
GeneReviews RCV000020456 SCV000040877 not provided Atelosteogenesis type III no assertion provided literature only

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