ClinVar Miner

Submissions for variant NM_000535.7(PMS2):c.706-20dup (rs60794673)

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Total submissions: 11
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
EGL Genetic Diagnostics,Eurofins Clinical Diagnostics RCV000179768 SCV000232072 benign not specified 2015-04-10 criteria provided, single submitter clinical testing
Division of Genomic Diagnostics,The Children's Hospital of Philadelphia RCV000202996 SCV000257704 benign Lynch syndrome 2015-05-11 criteria provided, single submitter clinical testing
Counsyl RCV000409009 SCV000488169 uncertain significance Hereditary nonpolyposis colorectal cancer type 4 2016-02-19 criteria provided, single submitter clinical testing
Quest Diagnostics Nichols Institute San Juan Capistrano RCV000179768 SCV000601856 benign not specified 2017-03-08 criteria provided, single submitter clinical testing
Invitae RCV000531203 SCV000625679 benign Hereditary nonpolyposis colorectal neoplasms 2017-07-18 criteria provided, single submitter clinical testing
Color RCV000582069 SCV000691103 benign Hereditary cancer-predisposing syndrome 2017-07-06 criteria provided, single submitter clinical testing
Color RCV000582069 SCV000691104 likely benign Hereditary cancer-predisposing syndrome 2017-07-25 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,University Medical Center Utrecht RCV000409009 SCV000743784 likely benign Hereditary nonpolyposis colorectal cancer type 4 2016-05-20 criteria provided, single submitter clinical testing
DNA and Cytogenetics Diagnostics Unit,Erasmus Medical Center RCV000409009 SCV000745195 benign Hereditary nonpolyposis colorectal cancer type 4 2017-06-28 criteria provided, single submitter clinical testing
Genome Diagnostics Laboratory,VU University Medical Center Amsterdam RCV000409009 SCV000745846 likely benign Hereditary nonpolyposis colorectal cancer type 4 2015-05-08 no assertion criteria provided clinical testing
Ding PR Lab,Sun Yat-sen University Cancer Center RCV001093662 SCV001250843 uncertain significance Lynch syndrome I no assertion criteria provided clinical testing

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