ClinVar Miner

Submissions for variant NM_014845.6(FIG4):c.1948+5G>T

dbSNP: rs756884619
Minimum review status: Collection method:
Minimum conflict level:
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000487985 SCV000575490 uncertain significance not provided 2016-11-01 criteria provided, single submitter clinical testing

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