ClinVar Miner

List of variants in gene FN1 reported as likely benign for fibronectin glomerulopathy

Included ClinVar conditions (3):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 60
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HGVS dbSNP gnomAD frequency
NM_212482.4(FN1):c.3189C>T (p.Thr1063=) rs78262627 0.00693
NM_212482.4(FN1):c.2130C>T (p.Thr710=) rs140116931 0.00113
NM_212482.4(FN1):c.416-17C>T rs142394008 0.00106
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.1023C>T (p.Ser341=) rs138120768 0.00063
NM_212482.4(FN1):c.2829C>T (p.Pro943=) rs112901124 0.00054
NM_212482.4(FN1):c.6336T>C (p.Pro2112=) rs148278567 0.00051
NM_212482.4(FN1):c.117C>G (p.Pro39=) rs148348956 0.00049
NM_212482.4(FN1):c.5623-13C>G rs192981567 0.00049
NM_212482.4(FN1):c.5761A>T (p.Ile1921Phe) rs138593265 0.00045
NM_212482.4(FN1):c.5164+14G>T rs186800160 0.00040
NM_212482.4(FN1):c.5532A>C (p.Arg1844=) rs149965879 0.00040
NM_212482.4(FN1):c.1676-9G>A rs372339259 0.00034
NM_212482.4(FN1):c.1860G>A (p.Pro620=) rs147845471 0.00031
NM_212482.4(FN1):c.2713+20A>G rs368435928 0.00027
NM_212482.4(FN1):c.2538G>A (p.Ser846=) rs145300210 0.00025
NM_212482.4(FN1):c.2896G>A (p.Gly966Arg) rs141400341 0.00021
NM_212482.4(FN1):c.3909T>G (p.Val1303=) rs200729428 0.00021
NM_212482.4(FN1):c.4791C>T (p.Ser1597=) rs374970848 0.00020
NM_212482.4(FN1):c.2413A>G (p.Thr805Ala) rs199957523 0.00019
NM_212482.4(FN1):c.2714-11_2714-10del rs371418810 0.00017
NM_212482.4(FN1):c.1820-16A>G rs72943927 0.00016
NM_212482.4(FN1):c.3012G>A (p.Gln1004=) rs142994783 0.00015
NM_212482.4(FN1):c.6158-7C>T rs372760499 0.00012
NM_212482.4(FN1):c.6459G>A (p.Pro2153=) rs372396685 0.00011
NM_212482.4(FN1):c.5051-9C>A rs376036111 0.00010
NM_212482.4(FN1):c.3492G>A (p.Ala1164=) rs548899134 0.00009
NM_212482.4(FN1):c.1413A>C (p.Thr471=) rs1009644782 0.00007
NM_212482.4(FN1):c.1871A>G (p.Asn624Ser) rs199764052 0.00007
NM_212482.4(FN1):c.6157+4T>C rs779209474 0.00006
NM_212482.4(FN1):c.3187A>G (p.Thr1063Ala) rs752617883 0.00005
NM_212482.4(FN1):c.4626G>A (p.Pro1542=) rs142628915 0.00005
NM_212482.4(FN1):c.6121C>T (p.Arg2041Trp) rs376754454 0.00005
NM_212482.4(FN1):c.247C>A (p.Arg83=) rs780120577 0.00004
NM_212482.4(FN1):c.2717C>T (p.Thr906Ile) rs370342980 0.00004
NM_212482.4(FN1):c.3866C>T (p.Pro1289Leu) rs751026014 0.00004
NM_212482.4(FN1):c.4559T>G (p.Val1520Gly) rs370343584 0.00004
NM_212482.4(FN1):c.6066C>T (p.Thr2022=) rs144324514 0.00004
NM_212482.4(FN1):c.1757A>G (p.Gln586Arg) rs138219703 0.00003
NM_212482.4(FN1):c.3288C>T (p.Thr1096=) rs754499962 0.00003
NM_212482.4(FN1):c.2299+16C>T rs201231230 0.00002
NM_212482.4(FN1):c.4719C>T (p.Tyr1573=) rs147150819 0.00002
NM_212482.4(FN1):c.5511T>C (p.Asn1837=) rs760293471 0.00002
NM_212482.4(FN1):c.548-10T>C rs1407477861 0.00001
NM_212482.4(FN1):c.665G>A (p.Arg222His) rs778971356 0.00001
NM_212482.4(FN1):c.1449G>A (p.Gln483=) rs749775069
NM_212482.4(FN1):c.148+16G>A rs367674539
NM_212482.4(FN1):c.1942-38GT[13] rs5838511
NM_212482.4(FN1):c.1942-38GT[14] rs5838511
NM_212482.4(FN1):c.2518+12G>C rs7570208
NM_212482.4(FN1):c.2714-10T>C
NM_212482.4(FN1):c.2967G>C (p.Leu989=) rs372040503
NM_212482.4(FN1):c.3091G>A (p.Val1031Met)
NM_212482.4(FN1):c.4012G>A (p.Val1338Ile)
NM_212482.4(FN1):c.6348C>A (p.His2116Gln)
NM_212482.4(FN1):c.6479T>C (p.Ile2160Thr)
NM_212482.4(FN1):c.6507G>A (p.Pro2169=) rs145436721
NM_212482.4(FN1):c.6507G>C (p.Pro2169=)
NM_212482.4(FN1):c.6634A>G (p.Ile2212Val) rs17449032

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