ClinVar Miner

Submissions for variant NM_033641.4(COL4A6):c.1952-2785_1952-2784insAGA

dbSNP: rs146680910
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Al Jalila Children’s Genomics Center, Al Jalila Childrens Speciality Hospital RCV001733580 SCV001984215 benign Hearing loss, X-linked 6 2020-01-08 criteria provided, single submitter clinical testing

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