ClinVar Miner

Submissions for variant NM_014314.4(RIGI):c.1481-21dup

dbSNP: rs71504272
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ClinVar version:
Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Genome-Nilou Lab RCV001661386 SCV001876624 benign Singleton-Merten syndrome 2 2021-07-30 criteria provided, single submitter clinical testing
Fulgent Genetics, Fulgent Genetics RCV001661386 SCV002802662 benign Singleton-Merten syndrome 2 2021-08-18 criteria provided, single submitter clinical testing

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