ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Endocrine oncology group, Uppsala University and "pathogenic" from any submitter

Minimum review status of the submission from Endocrine oncology group, Uppsala University: Collection method of the submission from Endocrine oncology group, Uppsala University:
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_001048174.2(MUTYH):c.1103G>A (p.Gly368Asp) rs36053993 0.00341

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