ClinVar Miner

List of variants reported as likely benign by ClinGen FBN1 Variant Curation Expert Panel, ClinGen

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)
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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_000138.5(FBN1):c.3058A>G (p.Thr1020Ala)	rs111801777	0.00029
NM_000138.5(FBN1):c.985A>G (p.Ile329Val)	rs370955295	0.00004
NM_000138.5(FBN1):c.3689T>C (p.Met1230Thr)	rs774003646	0.00001

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