ClinVar Miner

Submissions for variant NM_000169.3(GLA):c.915T>C (p.Pro305=)

dbSNP: rs782250167
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Color Diagnostics, LLC DBA Color Health RCV001184931 SCV001351028 likely benign Fabry disease 2019-11-06 criteria provided, single submitter clinical testing

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