ClinGen - ClinGen Clinical Genome Resource

ClinGen - ClinGen ClinGen, , ClinGen, ClinGen. ClinGen and ClinVar Partnership. ClinGen Curation Activities Overview. ClinGen Terms of Use. Working Groups and Expert Panels. Working Groups and Expert Panels. Clinical Domain Working Groups. Copy Number Variant Interpretation Guidelines. CADRe Consent and Disclosure Recommendations. Sequence Variant Inter-Laboratory Discrepancy Resolution. Clinical Domain Working Groups. Inborn Errors of Metabolism CDWG. All ClinGen Curation Groups. SomaticGermline Va.

OVERVIEW

The domain clinicalgenome.org presently has an average traffic classification of four hundred and thirty-six thousand seven hundred and twenty-five (the lower the superior). We have inspected twenty pages within the web site clinicalgenome.org and found forty-eight websites linking to clinicalgenome.org. There are two contacts and directions for clinicalgenome.org to help you contact them. There are one mass media accounts enjoyed by clinicalgenome.org. The domain clinicalgenome.org has been online for five hundred and ninety-one weeks, twenty hours, nine minutes, and fifty-one seconds.
Traffic Rank
#436725
Pages Crawled
20
Links to this site
48
Contacts
2
Addresses
2
Social Links
1
Online Since
Sep 2013

CLINICALGENOME.ORG TRAFFIC

The domain clinicalgenome.org is seeing fluctuating levels of traffic until the end of the year. Astonishingly, the web site had a ranking today of four hundred and thirty-six thousand seven hundred and twenty-five.
Traffic for clinicalgenome.org

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CLINICALGENOME.ORG HISTORY

The domain clinicalgenome.org was first documented on September 04, 2013. As of today, it is five hundred and ninety-one weeks, twenty hours, nine minutes, and fifty-one seconds young.
REGISTERED
September
2013

PERIOD

11
YEARS
4
MONTHS
0
DAYS

LINKS TO DOMAIN

ICCG has been moved to our new site, www.clinicalgenome.org.

All of the tools, content, etc. Has been moved to our new site, www. Please visit us there to continue using our resources. And for the latest information about ICCG! .

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In both research and clinical settings, the majority of patients with rare disease lack a clear etiology after exome and genome sequencing. Finding just a single additional case with a deleterious variant in the same gene and overlapping phenotype may provide sufficient evidence to identify the causative gene, but today, case data sits in isolated databases. Matchmaker Exchange Participants and Supporters. Mdash; Updated March 2015.

WHAT DOES CLINICALGENOME.ORG LOOK LIKE?

Desktop Screenshot of clinicalgenome.org Mobile Screenshot of clinicalgenome.org Tablet Screenshot of clinicalgenome.org

CONTACTS

Cherry Lab, Stanford Univ

Cherry Lab, Stanford Univ

Dept Genetics, Stanford University

Stanford, CA, 94305-5120

US

Cherry Lab, Stanford Univ

Cherry Lab, Stanford Univ

Dept Genetics, Stanford University

CLINICALGENOME.ORG SERVER

I revealed that a single root page on clinicalgenome.org took six hundred and eighty-three milliseconds to load. Our crawlers identified a SSL certificate, so therefore our web crawlers consider this site secure.
Load time
0.683 secs
SSL
SECURE
Internet Protocol
52.24.167.14

SERVER OS

We observed that clinicalgenome.org is using the Apache os.

HTML TITLE

ClinGen - ClinGen Clinical Genome Resource

DESCRIPTION

ClinGen - ClinGen ClinGen, , ClinGen, ClinGen. ClinGen and ClinVar Partnership. ClinGen Curation Activities Overview. ClinGen Terms of Use. Working Groups and Expert Panels. Working Groups and Expert Panels. Clinical Domain Working Groups. Copy Number Variant Interpretation Guidelines. CADRe Consent and Disclosure Recommendations. Sequence Variant Inter-Laboratory Discrepancy Resolution. Clinical Domain Working Groups. Inborn Errors of Metabolism CDWG. All ClinGen Curation Groups. SomaticGermline Va.

PARSED CONTENT

The domain states the following, "ClinGen - ClinGen ClinGen, , ClinGen, ClinGen." We analyzed that the web site also stated " Working Groups and Expert Panels." It also stated " Working Groups and Expert Panels. Copy Number Variant Interpretation Guidelines. CADRe Consent and Disclosure Recommendations. Sequence Variant Inter-Laboratory Discrepancy Resolution. Inborn Errors of Metabolism CDWG."

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