ClinVar Miner

Submissions for variant NM_006612.6(KIF1C):c.528G>A (p.Pro176=)

gnomAD frequency: 0.00004  dbSNP: rs775719793
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
Labcorp Genetics (formerly Invitae), Labcorp RCV002539264 SCV001021274 likely benign Spastic ataxia 2 2022-10-01 criteria provided, single submitter clinical testing

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