ClinVar Miner

Submissions for variant NM_005343.4(HRAS):c.171T>C (p.Asp57=)

gnomAD frequency: 0.00001  dbSNP: rs776105083
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Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000246927 SCV000311010 likely benign not specified criteria provided, single submitter clinical testing
Invitae RCV000871401 SCV001013057 likely benign Costello syndrome 2023-10-08 criteria provided, single submitter clinical testing
Sema4, Sema4 RCV002258867 SCV002537968 uncertain significance Hereditary cancer-predisposing syndrome 2022-03-04 criteria provided, single submitter curation

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