ClinVar Miner

Variants in gene FN1 with conflicting interpretations "likely benign" and "benign"

Submission 1 (likely benign) minimum review status: Submission 1 (likely benign) method:
Submission 2 (benign) minimum review status: Submission 2 (benign) method:
Gene type:
ClinVar version:
Total variants with conflicting interpretations: 26
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HGVS dbSNP gnomAD frequency
NM_212482.4(FN1):c.2592C>T (p.Ser864=) rs74574217 0.01052
NM_212482.4(FN1):c.1425G>C (p.Gly475=) rs59884263 0.01019
NM_212482.4(FN1):c.1530C>T (p.Ala510=) rs61263981 0.01017
NM_212482.4(FN1):c.3837C>T (p.Thr1279=) rs61732520 0.00656
NM_212482.4(FN1):c.121T>G (p.Ser41Ala) rs112946345 0.00576
NM_212482.4(FN1):c.4486C>T (p.Arg1496Trp) rs139078629 0.00542
NM_212482.4(FN1):c.199C>A (p.Arg67=) rs112643151 0.00519
NM_212482.4(FN1):c.4444C>T (p.Arg1482Cys) rs116558455 0.00146
NM_212482.4(FN1):c.751A>T (p.Asn251Tyr) rs55822567 0.00130
NM_212482.4(FN1):c.2130C>T (p.Thr710=) rs140116931 0.00113
NM_212482.4(FN1):c.547+19T>C rs183120644 0.00099
NM_212482.4(FN1):c.1002G>A (p.Thr334=) rs138271073 0.00094
NM_212482.4(FN1):c.3517+3A>G rs201910111 0.00073
NM_212482.4(FN1):c.5435-7T>C rs202045892 0.00068
NM_212482.4(FN1):c.5761A>T (p.Ile1921Phe) rs138593265 0.00045
NM_212482.4(FN1):c.887C>T (p.Pro296Leu) rs145123731 0.00045
NM_212482.4(FN1):c.5532A>C (p.Arg1844=) rs149965879 0.00040
NM_212482.4(FN1):c.547+10T>C rs376212853 0.00034
NM_212482.4(FN1):c.807G>A (p.Lys269=) rs149709418 0.00024
NM_212482.4(FN1):c.2144C>T (p.Thr715Met) rs144664306 0.00017
NM_212482.4(FN1):c.2714-11_2714-10del rs371418810 0.00017
NM_212482.4(FN1):c.4257C>T (p.Leu1419=) rs141157994 0.00010
NM_212482.4(FN1):c.1782T>C (p.Ile594=) rs201143720 0.00006
NM_212482.4(FN1):c.1942-38GT[9] rs5838511
NM_212482.4(FN1):c.5274G>T (p.Ser1758=) rs34923683
NM_212482.4(FN1):c.6634A>G (p.Ile2212Val) rs17449032

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