ClinVar Miner

Submissions for variant NM_000511.6(FUT2):c.772G>A (p.Gly258Ser)

gnomAD frequency: 0.47222  dbSNP: rs602662
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
University of Washington Center for Mendelian Genomics, University of Washington RCV001291127 SCV001479493 confers sensitivity Familial Otitis Media no assertion criteria provided research
Pharmacogenomics/Precision medicine lab, University of Petra RCV003316837 SCV004020297 other Levothyroxine response no assertion criteria provided research

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