ClinVar Miner

Submissions for variant NM_206965.2(FTCD):c.368-17G>A

dbSNP: rs61688555
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Labcorp Genetics (formerly Invitae), Labcorp RCV002145068 SCV002414973 benign Glutamate formiminotransferase deficiency 2023-08-29 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004714376 SCV005279679 benign not provided criteria provided, single submitter not provided

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