ClinVar Miner

Submissions for variant NM_012079.6(DGAT1):c.981+1G>T (rs781934305)

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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome Sciences and Precision Medicine Center,Medical College of Wisconsin RCV000844890 SCV000965589 likely pathogenic Diarrhea 7 2019-08-13 no assertion criteria provided clinical testing Clinically affected, compound heterozygote

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