ClinVar Miner

List of variants reported as likely pathogenic for Fanconi anemia complementation group U by Laboratorio de Genetica e Diagnostico Molecular, Hospital Israelita Albert Einstein

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 1
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HGVS dbSNP gnomAD frequency
NM_005431.2(XRCC2):c.378_381del (p.Leu126fs) rs763401560

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