ClinVar Miner

Submissions for variant NM_001099274.3(TINF2):c.710G>A (p.Gly237Asp) (rs17102313)

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Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories RCV000505877 SCV000605384 benign not specified 2017-04-04 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000310733 SCV000386426 benign Dyskeratosis Congenita, Dominant 2016-06-14 criteria provided, single submitter clinical testing
Illumina Clinical Services Laboratory,Illumina RCV000344620 SCV000386427 benign Revesz syndrome 2016-06-14 criteria provided, single submitter clinical testing
Invitae RCV000456519 SCV000557255 benign Dyskeratosis congenita 2018-01-08 criteria provided, single submitter clinical testing

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