ClinVar Miner

List of variants reported as uncertain significance for Klippel-Feil syndrome 1, autosomal dominant by UAEU Genomics Laboratory, United Arab Emirates University

Included ClinVar conditions (6):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001001557.4(GDF6):c.1304C>T (p.Ala435Val) rs140782427 0.00014

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