ClinVar Miner

List of variants reported as likely pathogenic for MAPK8IP3-related disorder by Undiagnosed Diseases Network, NIH

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_001318852.2(MAPK8IP3):c.111C>G (p.Tyr37Ter) rs770703007

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