ClinVar Miner

Submissions for variant NM_198525.3(KIF7):c.3582G>A (p.Glu1194=)

dbSNP: rs575165138
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000244993 SCV000316994 likely benign not specified criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002058477 SCV002415340 likely benign Acrocallosal syndrome 2022-07-05 criteria provided, single submitter clinical testing

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