ClinVar Miner

Variants with conflicting interpretations "pathogenic" from National Center for Biotechnology Information, National Institutes of Health and "likely pathogenic" from Fulgent Genetics, Fulgent Genetics

Minimum review status of the submission from National Center for Biotechnology Information, National Institutes of Health: Collection method of the submission from National Center for Biotechnology Information, National Institutes of Health:
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 gnomAD frequency
NM_000151.4(G6PC1):c.980_982del (p.Phe327del) rs80356486

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