ClinVar Miner

Variants with conflicting interpretations "pathogenic" from Muenke lab,National Institutes of Health and "uncertain significance" from any submitter

Minimum review status of the submission from Muenke lab,National Institutes of Health: Collection method of the submission from Muenke lab,National Institutes of Health:
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
NM_023110.2(FGFR1):c.1880G>C (p.Arg627Thr) rs869025671

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