ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.1896G>C (p.Gly632=)

gnomAD frequency: 0.00006  dbSNP: rs200859735
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
Invitae RCV000476867 SCV000558643 likely benign Fanconi anemia 2024-01-09 criteria provided, single submitter clinical testing
KCCC/NGS Laboratory, Kuwait Cancer Control Center RCV003316601 SCV004015514 likely benign Fanconi anemia complementation group P 2023-07-07 criteria provided, single submitter clinical testing

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