ClinVar Miner

Submissions for variant NM_000131.4(F7):c.64+8C>T (rs10482844)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Clinical Services Laboratory,Illumina RCV000377427 SCV000382732 likely benign Factor VII deficiency 2017-04-28 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases allowed determination this variant is unlikely to cause disease. Therefore, this variant is classified as likely benign.
Invitae RCV000890086 SCV001033811 benign not provided 2018-03-30 criteria provided, single submitter clinical testing

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