ClinVar Miner

Submissions for variant NM_006885.4(ZFHX3):c.10142_10165del (p.Arg3381_Gln3388del)

dbSNP: rs727502780
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
CeGaT Center for Human Genetics Tuebingen RCV000996316 SCV001150985 uncertain significance not provided 2017-02-01 criteria provided, single submitter clinical testing
Mendelics RCV002247371 SCV002516761 benign not specified 2022-05-04 criteria provided, single submitter clinical testing
OMIM RCV000019797 SCV000040095 pathogenic Prostate cancer, somatic 2005-04-01 no assertion criteria provided literature only

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