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

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:
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 3

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HGVS	dbSNP	gnomAD frequency
NM_017563.5(IL17RD):c.392A>C (p.Lys131Thr)	rs184758350	0.00063
NM_023110.3(FGFR1):c.1037_1038del (p.Ser346fs)	rs727505371
NM_023110.3(FGFR1):c.1864C>T (p.Arg622Ter)	rs121909628

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