ClinVar Miner

List of variants reported as benign for Familial visceral amyloidosis, Ostertag type by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000239.3(LYZ):c.*178C>T rs710794 0.89111
NM_021871.3(FGA):c.-58A>G rs2070011 0.65406
NM_000239.3(LYZ):c.*835C>T rs1384 0.40016
NM_021871.4(FGA):c.991A>G (p.Thr331Ala) rs6050 0.29256
NM_000239.3(LYZ):c.*655G>T rs8612 0.10799
NM_000239.3(LYZ):c.-1C>T rs513342 0.06603
NM_000239.3(LYZ):c.263C>A (p.Thr88Asn) rs1800973 0.04360
NM_000239.3(LYZ):c.*461G>A rs531233279 0.00770
NM_000039.3(APOA1):c.732C>G (p.Pro244=) rs5080 0.00368
NM_000239.3(LYZ):c.10C>G (p.Leu4Val) rs58131341 0.00302
NM_021871.4(FGA):c.1366A>G (p.Thr456Ala) rs2070031 0.00262
NM_021871.4(FGA):c.16A>G (p.Ile6Val) rs2070025 0.00250
NM_021871.4(FGA):c.181-14C>T rs190703077 0.00240
NM_021871.4(FGA):c.300G>A (p.Lys100=) rs112877216 0.00240
NM_000239.3(LYZ):c.*890T>C rs188271229 0.00204
NM_000239.3(LYZ):c.*418C>A rs534565279 0.00177
NM_000239.3(LYZ):c.*415G>A rs183441118 0.00159
NM_000239.3(LYZ):c.*413G>T rs193040437 0.00128
NM_000239.3(LYZ):c.*169G>A rs568058282 0.00126
NM_000239.3(LYZ):c.*191A>G rs183375295 0.00101
NM_000039.3(APOA1):c.181G>A (p.Ala61Thr) rs12718465 0.00091
NM_000039.3(APOA1):c.562G>T (p.Ala188Ser) rs140770089 0.00058
NM_021871.4(FGA):c.1417G>A (p.Asp473Asn) rs200378626 0.00048
NM_000039.3(APOA1):c.178T>G (p.Ser60Ala) rs199759119 0.00043
NM_021871.4(FGA):c.1199C>T (p.Ser400Phe) rs184635235 0.00031
NM_021871.4(FGA):c.244A>C (p.Thr82Pro) rs199554805 0.00031
NM_000039.3(APOA1):c.*19C>G rs187335584 0.00029
NM_021871.4(FGA):c.*50T>G rs369606098 0.00010
NM_021871.4(FGA):c.1072G>A (p.Gly358Arg) rs201105899 0.00007
NM_000039.3(APOA1):c.9T>C (p.Ala3=) rs141383703 0.00006
NM_021871.4(FGA):c.1838A>G (p.His613Arg) rs201686865 0.00004
NM_000039.3(APOA1):c.28G>A (p.Val10Met) rs750125257 0.00003
NM_021871.4(FGA):c.1718G>A (p.Arg573His) rs78506343 0.00003
NM_000239.3(LYZ):c.151A>T (p.Lys51Ter) rs367682582 0.00002
NM_021871.4(FGA):c.1918C>G (p.Pro640Ala) rs199571440 0.00002
NM_021871.4(FGA):c.450G>A (p.Gln150=) rs368446857 0.00002
NM_021871.4(FGA):c.904C>G (p.Pro302Ala) rs200203992 0.00002
NM_021871.4(FGA):c.1912G>A (p.Gly638Arg) rs771429165 0.00001
NM_000239.3(LYZ):c.*266G>A rs188313797
NM_000239.3(LYZ):c.*521G>A rs567541896
NM_000239.3(LYZ):c.415G>C (p.Val139Leu) rs367623154
NM_021871.4(FGA):c.*133G>A rs182736373

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.