ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Forensic Genetics Laboratory, Harris County Institute of Forensic Sciences and "likely pathogenic" from any submitter

Minimum review status of the submission from Forensic Genetics Laboratory, Harris County Institute of Forensic Sciences: Collection method of the submission from Forensic Genetics Laboratory, Harris County Institute of Forensic Sciences:
Minimum review status of the other submission: Collection method of the other submission:
ClinVar version:
Total variants with conflicting interpretations: 2
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HGVS dbSNP gnomAD frequency
NM_015141.4(GPD1L):c.839C>T (p.Ala280Val) rs72552291 0.00011
NM_000432.4(MYL2):c.64G>A (p.Glu22Lys) rs104894368

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