ClinVar Miner

List of variants in gene FGF23 reported as uncertain significance for tumoral calcinosis, hyperphosphatemic, familial, 2

Included ClinVar conditions (2):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 69
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HGVS dbSNP gnomAD frequency
NM_020638.3(FGF23):c.*1772G>A rs13312800 0.00298
NM_020638.3(FGF23):c.*1886C>A rs183802802 0.00169
NM_020638.3(FGF23):c.*1575T>C rs562433374 0.00088
NM_020638.3(FGF23):c.*235C>T rs566868058 0.00064
NM_020638.3(FGF23):c.*784C>T rs553998728 0.00022
NM_020638.3(FGF23):c.*1398T>A rs531815578 0.00019
NM_020638.3(FGF23):c.551A>G (p.Asp184Gly) rs144925325 0.00019
NM_020638.3(FGF23):c.*1492T>C rs986708682 0.00014
NM_020638.3(FGF23):c.*1803C>T rs13312801 0.00012
NM_020638.3(FGF23):c.559C>G (p.Arg187Gly) rs190841442 0.00007
NM_020638.3(FGF23):c.88C>T (p.Pro30Ser) rs758725402 0.00006
NM_020638.3(FGF23):c.*181T>C rs886049409 0.00005
NM_020638.3(FGF23):c.331G>A (p.Glu111Lys) rs765478662 0.00005
NM_020638.3(FGF23):c.*1049C>T rs13312797 0.00004
NM_020638.3(FGF23):c.636C>A (p.Ser212Arg) rs749770315 0.00004
NM_020638.3(FGF23):c.*1292C>T rs897877189 0.00003
NM_020638.3(FGF23):c.*1352T>C rs886049398 0.00003
NM_020638.3(FGF23):c.*182G>A rs563817819 0.00003
NM_020638.3(FGF23):c.*856C>G rs886049399 0.00003
NM_020638.3(FGF23):c.-23C>T rs769953313 0.00003
NM_020638.3(FGF23):c.64C>T (p.Leu22Phe) rs376694108 0.00003
NM_020638.3(FGF23):c.73T>C (p.Tyr25His) rs769336439 0.00003
NM_020638.3(FGF23):c.*944G>A rs561820380 0.00002
NM_020638.3(FGF23):c.249G>A (p.Val83=) rs753676774 0.00002
NM_020638.3(FGF23):c.46G>A (p.Val16Ile) rs760118094 0.00002
NM_020638.3(FGF23):c.*1134A>T rs1865034354 0.00001
NM_020638.3(FGF23):c.*1925A>G rs886049397 0.00001
NM_020638.3(FGF23):c.*614G>A rs886049401 0.00001
NM_020638.3(FGF23):c.*93G>A rs886049410 0.00001
NM_020638.3(FGF23):c.138A>G (p.Thr46=) rs368115734 0.00001
NM_020638.3(FGF23):c.457C>G (p.Pro153Ala) rs774018822 0.00001
NM_020638.3(FGF23):c.515C>T (p.Pro172Leu) rs573322878 0.00001
NM_020638.3(FGF23):c.57G>A (p.Met19Ile) rs766148024 0.00001
NM_020638.3(FGF23):c.673G>A (p.Gly225Arg) rs750025882 0.00001
NM_020638.3(FGF23):c.*1548T>G rs762018989
NM_020638.3(FGF23):c.*278G>C rs886049408
NM_020638.3(FGF23):c.*28C>G rs886049411
NM_020638.3(FGF23):c.*460A>T rs775907152
NM_020638.3(FGF23):c.*664A>T rs886049400
NM_020638.3(FGF23):c.-111C>T rs1865158291
NM_020638.3(FGF23):c.-55C>A rs760895385
NM_020638.3(FGF23):c.133G>A (p.Ala45Thr)
NM_020638.3(FGF23):c.13C>T (p.Arg5Cys)
NM_020638.3(FGF23):c.210_211del (p.Tyr70_Ser71delinsTer)
NM_020638.3(FGF23):c.211+12T>G rs1865152731
NM_020638.3(FGF23):c.277T>C (p.Tyr93His)
NM_020638.3(FGF23):c.313T>A (p.Ser105Thr) rs1865075955
NM_020638.3(FGF23):c.329C>T (p.Pro110Leu)
NM_020638.3(FGF23):c.330G>A (p.Pro110=)
NM_020638.3(FGF23):c.414G>C (p.Leu138=) rs1865054870
NM_020638.3(FGF23):c.428G>A (p.Arg143Lys)
NM_020638.3(FGF23):c.446T>C (p.Met149Thr)
NM_020638.3(FGF23):c.486C>G (p.Asn162Lys)
NM_020638.3(FGF23):c.529C>A (p.His177Asn)
NM_020638.3(FGF23):c.544G>A (p.Glu182Lys)
NM_020638.3(FGF23):c.550G>A (p.Asp184Asn)
NM_020638.3(FGF23):c.559C>T (p.Arg187Trp) rs190841442
NM_020638.3(FGF23):c.60C>T (p.Ser20=) rs763114180
NM_020638.3(FGF23):c.61G>A (p.Val21Ile)
NM_020638.3(FGF23):c.637G>A (p.Ala213Thr)
NM_020638.3(FGF23):c.640G>A (p.Glu214Lys)
NM_020638.3(FGF23):c.685G>T (p.Gly229Cys)
NM_020638.3(FGF23):c.686G>A (p.Gly229Asp) rs1033823201
NM_020638.3(FGF23):c.688G>A (p.Gly230Ser)
NM_020638.3(FGF23):c.706G>C (p.Ala236Pro)
NM_020638.3(FGF23):c.725A>G (p.Glu242Gly)
NM_020638.3(FGF23):c.742G>A (p.Ala248Thr)
NM_020638.3(FGF23):c.746A>T (p.Lys249Met)
NM_020638.3(FGF23):c.751A>G (p.Ile251Val)

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