ClinVar Miner

Submissions for variant NM_005360.5(MAF):c.-30GGC[7]

dbSNP: rs5818251
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 4
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
PreventionGenetics, part of Exact Sciences RCV000254425 SCV000311020 benign not specified criteria provided, single submitter clinical testing
GeneDx RCV001610662 SCV001841579 benign not provided 2019-08-15 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775745 SCV002014080 benign Ayme-Gripp syndrome 2021-09-05 criteria provided, single submitter clinical testing
Genome-Nilou Lab RCV001775744 SCV002014081 benign Cataract 21 multiple types 2021-09-05 criteria provided, single submitter clinical testing

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