ClinVar Miner

Submissions for variant NM_001204286.1(MUC1):c.93G>A (p.Thr31=)

gnomAD frequency: 0.58553  dbSNP: rs4072037
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001775529 SCV002014301 benign Tubulointerstitial kidney disease, autosomal dominant, 2 2021-09-05 criteria provided, single submitter clinical testing
Breakthrough Genomics, Breakthrough Genomics RCV004715549 SCV005282198 benign not provided criteria provided, single submitter not provided

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