ClinVar Miner

Submissions for variant NM_000377.3(WAS):c.210G>A (p.Gly70=)

dbSNP: rs886038288
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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 RCV000246564 SCV000303900 likely benign not specified criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316347 SCV004016220 likely benign Wiskott-Aldrich syndrome 2023-07-07 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV003765497 SCV004603519 likely benign X-linked severe congenital neutropenia; Thrombocytopenia 1; Wiskott-Aldrich syndrome 2023-09-08 criteria provided, single submitter clinical testing

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