ClinVar Miner

Submissions for variant NM_015238.3(WWC1):c.1185-3222C>T

gnomAD frequency: 0.43508  dbSNP: rs17070145
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Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000088686 SCV000121608 association Memory quantitative trait locus 2013-08-07 no assertion criteria provided literature only

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