ClinVar Miner

List of variants in gene MED13L reported as likely pathogenic by University of Washington Center for Mendelian Genomics, University of Washington

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_015335.5(MED13L):c.4076G>A (p.Trp1359Ter) rs1592919048

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