ClinVar Miner

Submissions for variant NM_000504.4(F10):c.865+33A>G

gnomAD frequency: 0.93642  dbSNP: rs2031184
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001687936 SCV001910413 benign not provided 2021-06-18 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001702244 SCV001933652 benign Hereditary factor X deficiency disease 2021-08-10 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001687936 SCV005232096 benign not provided criteria provided, single submitter not provided

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