ClinVar Miner

Submissions for variant NM_001330574.2(ZNF711):c.*632A>G

gnomAD frequency: 0.22070  dbSNP: rs6653049
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000349795 SCV000482861 benign Non-syndromic X-linked intellectual disability 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000358346 SCV000484390 benign Premature ovarian failure 2B 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV001168454 SCV001331045 benign Intellectual disability, X-linked 97 2017-04-27 criteria provided, single submitter clinical testing This variant was observed as part of a predisposition screen in an ostensibly healthy population. A literature search was performed for the gene, cDNA change, and amino acid change (where applicable). No publications were found based on this search. Allele frequency data from public databases was too high to be consistent with this variant causing disease. Therefore, this variant is classified as benign.

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