ClinVar Miner

List of variants in gene combination FN1, LOC126806497 reported as likely benign for Inborn genetic diseases

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Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
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_212482.4(FN1):c.4114G>A (p.Asp1372Asn)	rs151236899	0.00040
NM_212482.4(FN1):c.4141C>T (p.Pro1381Ser)	rs754336717	0.00001

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