ClinVar Miner

List of variants in gene FN1 reported as uncertain significance for bone disorder

Included ClinVar conditions (1350):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 56
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HGVS dbSNP gnomAD frequency
NM_212482.4(FN1):c.3199G>A (p.Val1067Met) rs145483591 0.00021
NM_212482.4(FN1):c.141A>C (p.Gln47His) rs145263539 0.00019
NM_212482.4(FN1):c.4262C>G (p.Pro1421Arg) rs146898035 0.00016
NM_212482.4(FN1):c.2879C>G (p.Thr960Ser) rs565714281 0.00011
NM_212482.4(FN1):c.3020A>G (p.Asn1007Ser) rs145838840 0.00010
NM_212482.4(FN1):c.3130G>A (p.Val1044Met) rs34043251 0.00010
NM_212482.4(FN1):c.869G>A (p.Arg290His) rs150990682 0.00010
NM_212482.4(FN1):c.5741C>A (p.Thr1914Lys) rs765428225 0.00009
NM_212482.4(FN1):c.1871A>G (p.Asn624Ser) rs199764052 0.00007
NM_212482.4(FN1):c.3415G>A (p.Val1139Ile) rs201181695 0.00007
NM_212482.4(FN1):c.3289G>A (p.Glu1097Lys) rs753807100 0.00006
NM_212482.4(FN1):c.4801C>T (p.Pro1601Ser) rs532827189 0.00006
NM_212482.4(FN1):c.5482A>G (p.Ser1828Gly) rs199941833 0.00006
NM_212482.4(FN1):c.6052C>T (p.Arg2018Cys) rs372237449 0.00006
NM_212482.4(FN1):c.6157+4T>C rs779209474 0.00006
NM_212482.4(FN1):c.862G>A (p.Asp288Asn) rs200731330 0.00006
NM_212482.4(FN1):c.6121C>T (p.Arg2041Trp) rs376754454 0.00005
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.3968A>G (p.Tyr1323Cys) rs200891393 0.00004
NM_212482.4(FN1):c.4879A>G (p.Ile1627Val) rs370180533 0.00004
NM_212482.4(FN1):c.6784A>G (p.Ile2262Val) rs1330217896 0.00004
NM_212482.4(FN1):c.1757A>G (p.Gln586Arg) rs138219703 0.00003
NM_212482.4(FN1):c.3061C>T (p.Arg1021Trp) rs748276504 0.00003
NM_212482.4(FN1):c.4858G>A (p.Ala1620Thr) rs766780476 0.00003
NM_212482.4(FN1):c.5237C>T (p.Pro1746Leu) rs923283804 0.00003
NM_212482.4(FN1):c.5608G>T (p.Val1870Leu) rs375667567 0.00003
NM_212482.4(FN1):c.6506C>T (p.Pro2169Leu) rs755984905 0.00003
NM_212482.4(FN1):c.592G>A (p.Gly198Arg) rs561607931 0.00002
NM_212482.4(FN1):c.790G>A (p.Gly264Ser) rs950443871 0.00002
NM_212482.4(FN1):c.907C>T (p.Pro303Ser) rs750138959 0.00002
NM_212482.4(FN1):c.1544G>A (p.Arg515Gln) rs376696206 0.00001
NM_212482.4(FN1):c.2429C>T (p.Ala810Val) rs568343071 0.00001
NM_212482.4(FN1):c.3271A>G (p.Ile1091Val) rs80101897 0.00001
NM_212482.4(FN1):c.3959T>C (p.Val1320Ala) rs770129874 0.00001
NM_212482.4(FN1):c.4473A>T (p.Arg1491Ser) rs2059079828 0.00001
NM_212482.4(FN1):c.4558G>A (p.Val1520Ile) rs201469351 0.00001
NM_212482.4(FN1):c.4586C>G (p.Pro1529Arg) rs760993609 0.00001
NM_212482.4(FN1):c.4720G>A (p.Gly1574Arg) rs764285223 0.00001
NM_212482.4(FN1):c.5602G>A (p.Val1868Met) rs369072643 0.00001
NM_212482.4(FN1):c.5659A>G (p.Lys1887Glu) rs145946514 0.00001
NM_212482.4(FN1):c.5735G>A (p.Arg1912His) rs775421803 0.00001
NM_212482.4(FN1):c.6547G>T (p.Glu2183Ter) rs754396418 0.00001
NM_212482.4(FN1):c.665G>A (p.Arg222His) rs778971356 0.00001
NM_212482.4(FN1):c.749A>C (p.Asp250Ala) rs372163398 0.00001
NM_212482.4(FN1):c.1436G>T (p.Arg479Leu) rs761729774
NM_212482.4(FN1):c.1481T>C (p.Met494Thr) rs2064511350
NM_212482.4(FN1):c.1888T>G (p.Trp630Gly) rs2106350896
NM_212482.4(FN1):c.2150C>G (p.Pro717Arg) rs770505069
NM_212482.4(FN1):c.2299+3A>T rs2062278053
NM_212482.4(FN1):c.2422ACA[1] (p.Thr809del) rs1553636502
NM_212482.4(FN1):c.2605G>A (p.Asp869Asn)
NM_212482.4(FN1):c.3149A>C (p.Lys1050Thr) rs144581583
NM_212482.4(FN1):c.4649C>A (p.Ala1550Glu) rs202245868
NM_212482.4(FN1):c.5164+3A>G rs2105944563
NM_212482.4(FN1):c.5369_5370del (p.Thr1790fs) rs771111687

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