ClinVar Miner

List of variants reported as likely pathogenic for lymphangioma

Included ClinVar conditions (8):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
46;XX;t(6;17)(q13;q21)dn
NM_001142864.4(PIEZO1):c.5040C>A (p.Tyr1680Ter)
NM_006218.4(PIK3CA):c.3140A>T (p.His1047Leu)	rs121913279
NM_080680.3(COL11A2):c.966dup (p.Thr323fs)	rs748440351

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