ClinVar Miner

List of variants reported as uncertain significance for X-linked disease by Tolun Lab, Human Genetics Laboratory, Bogazici University

Included ClinVar conditions (275):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001256789.3(CACNA1F):c.1933A>T (p.Ile645Phe) rs1344295491

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