ClinVar Miner

Submissions for variant NM_020928.2(ZSWIM6):c.498A>G (p.Ala166=)

dbSNP: rs964738831
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Invitae RCV002126110 SCV002452966 likely benign not provided 2022-09-27 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV002494420 SCV002796639 likely benign Acromelic frontonasal dysostosis; Neurodevelopmental disorder with movement abnormalities, abnormal gait, and autistic features 2021-09-16 criteria provided, single submitter clinical testing

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