ClinVar Miner

Submissions for variant NM_005577.4(LPA):c.3947+467T>C

gnomAD frequency: 0.04383 dbSNP: rs10455872

Minimum review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
		ClinVar version:

Total submissions: 1

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Submitter	RCV	SCV	Clinical significance	Condition	Last evaluated	Review status	Method	Comment
OMIM	RCV001251438	SCV001427045	benign	LIPOPROTEIN(a) POLYMORPHISM	2020-08-07	no assertion criteria provided	literature only

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