ClinVar Miner

Submissions for variant NM_001025295.3(IFITM5):c.288G>A (p.Pro96=)

gnomAD frequency: 0.00006  dbSNP: rs149676171
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 RCV002071430 SCV002322749 likely benign not provided 2024-05-23 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002071430 SCV005220852 likely benign not provided criteria provided, single submitter not provided

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