ClinVar Miner

Submissions for variant NM_000237.3(LPL):c.1302A>T (p.Lys434Asn)

dbSNP: rs587777908
Minimum review status: Collection method:
Minimum conflict level:
ClinVar version:
Total submissions: 1
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Submitter RCV SCV Clinical significance Condition Last evaluated Review status Method Comment
idemuth, Charité - Universiätsmedizin Berlin RCV000145433 SCV000192464 not provided Hyperlipoproteinemia, type I no assertion provided not provided

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