ClinVar Miner

List of variants reported as benign for anencephaly by Genome-Nilou Lab

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001300759.2(TRIM36):c.1797-35T>G	rs2921623	0.99007
NM_001300759.2(TRIM36):c.1996G>A (p.Asp666Asn)	rs2974617	0.93155

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