ClinVar Miner

List of variants in gene KIF14 reported as likely pathogenic for Meckel syndrome

Included ClinVar conditions (40):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_014875.3(KIF14):c.1514T>C (p.Leu505Pro) rs1660016633

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