ClinVar Miner

Variants with conflicting interpretations "uncertain significance" from Institute of Human Genetics, Univ. Regensburg,Univ. Regensburg and "pathogenic" from any submitter

Minimum review status of the submission from Institute of Human Genetics, Univ. Regensburg,Univ. Regensburg: Collection method of the submission from Institute of Human Genetics, Univ. Regensburg,Univ. Regensburg:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 1
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HGVS dbSNP
NM_000350.3(ABCA4):c.4539+2028C>T rs869320785

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