ClinVar Miner

Submissions for variant NM_006019.4(TCIRG1):c.1887+175A>G

dbSNP: rs2075609
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001690111 SCV001910482 benign not provided 2018-11-12 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV001690111 SCV005319208 benign not provided criteria provided, single submitter not provided
Natera, Inc. RCV001832857 SCV002094922 benign Autosomal recessive osteopetrosis 1 2019-08-29 no assertion criteria provided clinical testing

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