ClinVar Miner

List of variants reported as likely pathogenic for bifid nose

Included ClinVar conditions (4):

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001379081.2(FREM1):c.631C>T (p.Gln211Ter)	rs990411562	0.00001
NM_001379081.2(FREM1):c.2097_2100del (p.Lys699fs)	rs769407804

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