ClinVar Miner

Submissions for variant NM_001065.3(TNFRSF1A):c.625+10A>G (rs1800693)

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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics,ARUP Laboratories RCV000244183 SCV000605406 benign not specified 2016-02-10 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000338370 SCV000380679 likely benign Familial Periodic Fever 2016-06-14 criteria provided, single submitter clinical testing
Laboratory for Molecular Medicine,Partners HealthCare Personalized Medicine RCV000244183 SCV000540559 benign not specified 2016-03-28 criteria provided, single submitter clinical testing Variant identified in a genome or exome case(s) and assessed due to predicted null impact of the variant or pathogenic assertions in the literature or databases. Disclaimer: This variant has not undergone full assessment. The following are preliminary notes: Frequency, one paper claims association with MS
OMIM RCV000030698 SCV000053359 risk factor Multiple sclerosis, susceptibility to, 5 2012-08-23 no assertion criteria provided literature only
PreventionGenetics RCV000244183 SCV000306335 benign not specified criteria provided, single submitter clinical testing

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