ClinVar Miner

List of variants reported as pathogenic for anencephaly

Included ClinVar conditions (6):

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001300759.2(TRIM36):c.1486C>A (p.Pro496Thr)	rs773607884	0.00002
NM_001378615.1(CC2D2A):c.4179+1del	rs386833760
NM_030952.3(NUAK2):c.412_433delinsG (p.Tyr138_Gln145delinsGlu)	rs2102647752

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