ClinVar Miner

Submissions for variant NC_000020.11:g.10674058G>T

dbSNP: rs191409481
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Illumina Laboratory Services, Illumina RCV000403009 SCV000483944 likely benign Isolated Nonsyndromic Congenital Heart Disease 2016-06-14 criteria provided, single submitter clinical testing
Illumina Laboratory Services, Illumina RCV000314620 SCV000483945 likely benign Arteriohepatic dysplasia 2016-06-14 criteria provided, single submitter clinical testing

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