ClinVar Miner

Submissions for variant NM_000452.3(SLC10A2):c.292G>A (p.Val98Ile)

gnomAD frequency: 0.02814  dbSNP: rs55971546
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 3
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Eurofins Ntd Llc (ga) RCV000728363 SCV000855922 benign not specified 2017-07-20 criteria provided, single submitter clinical testing
Labcorp Genetics (formerly Invitae), Labcorp RCV002533093 SCV003245715 benign not provided 2025-02-03 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV002533093 SCV005236076 benign not provided criteria provided, single submitter not provided

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