ClinVar Miner

Variants with conflicting interpretations "likely pathogenic" from Chan Lab, Boston Children's Hospital and "pathogenic" from OMIM

Minimum review status of the submission from Chan Lab, Boston Children's Hospital: Collection method of the submission from Chan Lab, Boston Children's Hospital:
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_017563.5(IL17RD):c.392A>C (p.Lys131Thr) rs184758350 0.00063

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