ClinVar Miner

Variants with conflicting interpretations "pathogenic" from University of Washington Center for Mendelian Genomics, University of Washington and "likely pathogenic" from any submitter

Minimum review status of the submission from University of Washington Center for Mendelian Genomics, University of Washington: Collection method of the submission from University of Washington Center for Mendelian Genomics, University of Washington:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 3
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HGVS dbSNP gnomAD frequency
NM_001142730.3(KCTD1):c.2009G>A (p.Gly670Asp) rs587777003
NM_020928.2(ZSWIM6):c.3487C>T (p.Arg1163Trp) rs587777695
NM_052867.4(NALCN):c.3542G>A (p.Arg1181Gln) rs786201003

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