ClinVar Miner

Submissions for variant NM_000511.6(FUT2):c.461G>A (p.Trp154Ter)

gnomAD frequency: 0.45281  dbSNP: rs601338
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Total submissions: 5
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Breakthrough Genomics, Breakthrough Genomics RCV004716906 SCV005313405 benign not provided criteria provided, single submitter not provided
Fulgent Genetics, Fulgent Genetics RCV002490360 SCV002799025 benign VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1; Bombay phenotype 2021-08-12 criteria provided, single submitter clinical testing
University of Washington Center for Mendelian Genomics, University of Washington RCV001291126 SCV001479492 confers sensitivity Familial Otitis Media no assertion criteria provided research
OMIM RCV000013810 SCV000034057 association VITAMIN B12 PLASMA LEVEL QUANTITATIVE TRAIT LOCUS 1 2008-10-01 no assertion criteria provided literature only
OMIM RCV000013808 SCV000034055 benign SECRETOR/NONSECRETOR POLYMORPHISM 2008-10-01 no assertion criteria provided literature only

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