ClinVar Miner

Submissions for variant NM_181776.3(SLC36A2):c.164+1G>A

gnomAD frequency: 0.00002  dbSNP: rs371203963
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Total submissions: 2
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
OMIM RCV000002485 SCV000022643 affects Hyperglycinuria 2008-12-01 no assertion criteria provided literature only
OMIM RCV000002486 SCV000022644 affects Iminoglycinuria 2008-12-01 no assertion criteria provided literature only

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