ClinVar Miner

Submissions for variant NM_198060.4(NRAP):c.*7del

gnomAD frequency: 0.35956  dbSNP: rs3832698
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000402418 SCV000360517 likely benign Factor VII Marburg I Variant Thrombophilia 2016-06-14 criteria provided, single submitter clinical testing
GeneDx RCV001642922 SCV001860819 benign not provided 2021-05-04 criteria provided, single submitter clinical testing

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