ClinVar Miner

Submissions for variant NM_001256760.2(HTR2C):c.-850C>T

gnomAD frequency: 0.12950  dbSNP: rs3813929
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
GeneDx RCV001770161 SCV002004800 likely benign not provided 2018-08-14 criteria provided, single submitter clinical testing This variant is associated with the following publications: (PMID: 15741483, 17376412, 21391883, 18192901, 19106782, 20010450, 20453482, 10768099)

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