Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1005300
rs1005300
CBX7
G 0.700 GeneticVariation GWASCAT Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma. 28025584

2017
dbSNP: rs10507419
rs10507419
LINC00457 ; LINC02343
A 0.700 GeneticVariation GWASCAT Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. 28679651

2017
dbSNP: rs10799599
rs10799599 		C 0.700 GeneticVariation GWASCAT Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma. 28025584

2017
dbSNP: rs4487645
rs4487645
DNAH11
C 0.700 GeneticVariation GWASCAT Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma. 28025584

2017
dbSNP: rs6752376
rs6752376
LOC105373401
T 0.700 GeneticVariation GWASCAT Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. 28679651

2017
dbSNP: rs7820212
rs7820212 		A 0.700 GeneticVariation GWASCAT Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. 28679651

2017
dbSNP: rs79419269
rs79419269
SMARCD3
C 0.700 GeneticVariation GWASCAT Genome-wide association study of immunoglobulin light chain amyloidosis in three patient cohorts: comparison with myeloma. 28025584

2017
dbSNP: rs9344
rs9344
CCND1
G 0.700 GeneticVariation GWASCAT Genome-wide association study of clinical parameters in immunoglobulin light chain amyloidosis in three patient cohorts. 28679651

2017
dbSNP: rs9344
rs9344
CCND1
G 0.700 GeneticVariation GWASCAT In AL amyloidosis, rs9344 at the splice site of cyclin D1, promoting translocation (11;14), reached the highest significance, P=7.80 × 10<sup>-11</sup>; the SNP was only marginally significant in MM. 28025584

2017
dbSNP: rs387907272
rs387907272
MYD88
0.010 GeneticVariation BEFREE We identified the MYD88 L265P somatic variant in cases with WM (39/42), MGUS (8/18), NHL (14/41, including 4/13 diffuse large B cell lymphoma (DLBCL), 1/8 mucosa-associated lymphoid tissue, 3/6 splenic marginal zone lymphoma (SMZL), 1/4 chronic lymphocytic leukemia, 2/3 nodal marginal zone lymphoma (NMZL), 1/2 mantle cell lymphoma, 1 Burkitt lymphoma, and 1 B cell NHL that could not be classified), primary AL (2/2), and IgM-PN (1/1). 28280994

2017
dbSNP: rs76992529
rs76992529
TTR
0.010 GeneticVariation BEFREE Cardiac amyloidosis in African Americans: comparison of clinical and laboratory features of transthyretin V122I amyloidosis and immunoglobulin light chain amyloidosis. 19781421

2009
dbSNP: rs121909612
rs121909612
FGA
0.010 GeneticVariation BEFREE The mutation underlying Glu526Val fibrinogen alpha-chain amyloidosis is incompletely penetrant and has a variable phenotype that can clinically mimic AL amyloidosis. 10825402

2000