ClinVar Miner

Submissions for variant NM_032444.4(SLX4):c.4604G>A (p.Gly1535Glu)

gnomAD frequency: 0.00001  dbSNP: rs1425908713
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ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
Caryl and Israel Englander Institute for Precision Medicine, Weill Cornell Medicine RCV002223164 SCV002500985 uncertain significance not specified no assertion criteria provided literature only

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