ClinVar Miner

List of variants reported as likely benign for bifid nose by 3billion

Included ClinVar conditions (4):

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_001379081.2(FREM1):c.4069G>A (p.Gly1357Arg)	rs775399423	0.00015
NM_001379081.2(FREM1):c.-12G>C	rs375233918	0.00001

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