ClinVar Miner

Submissions for variant NM_000634.3(CXCR1):c.827G>C (p.Ser276Thr)

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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV003973791 SCV004798549 benign CXCR1-related disorder 2019-12-09 criteria provided, single submitter clinical testing This variant is classified as benign based on ACMG/AMP sequence variant interpretation guidelines (Richards et al. 2015 PMID: 25741868, with internal and published modifications).
Department of Surgery, Campus Charité Mitte | Campus Virchow-klinikum, Charite-Universitaetsmedizin Berlin RCV003312796 SCV004011743 other Cholangiocarcinoma 2022-12-10 no assertion criteria provided research No association with disease-free or overall survival after resection of intrahepatic Cholangiocarcinoma

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