Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs104893751
rs104893751
OGG1
A 0.700 CausalMutation CLINVAR

dbSNP: rs137853236
rs137853236
HNF1A
T 0.700 CausalMutation CLINVAR

dbSNP: rs137853247
rs137853247
HNF1A ; HNF1A-AS1
A 0.700 CausalMutation CLINVAR

dbSNP: rs1397145500
rs1397145500
ERN1
0.700 GeneticVariation UNIPROT

dbSNP: rs147608663
rs147608663
RIOK2 ; LIX1-AS1
0.700 GeneticVariation UNIPROT

dbSNP: rs1555212014
rs1555212014
HNF1A
T 0.700 CausalMutation CLINVAR

dbSNP: rs372947534
rs372947534
FLT4
0.700 GeneticVariation UNIPROT

dbSNP: rs397516440
rs397516440
VHL
G 0.700 GeneticVariation CLINVAR

dbSNP: rs5030820
rs5030820
VHL
T 0.700 CausalMutation CLINVAR

dbSNP: rs555607708
rs555607708
CHEK2
A 0.700 CausalMutation CLINVAR

dbSNP: rs587776825
rs587776825
HNF1A
GC 0.700 CausalMutation CLINVAR

dbSNP: rs587782274
rs587782274
ATM ; C11orf65
0.700 GeneticVariation UNIPROT

dbSNP: rs754729248
rs754729248
HNF1A
G 0.700 CausalMutation CLINVAR

dbSNP: rs758175953
rs758175953
FLCN
A 0.700 GeneticVariation CLINVAR

dbSNP: rs78683075
rs78683075
FLCN
0.700 GeneticVariation UNIPROT

dbSNP: rs864321679
rs864321679
PBRM1 ; SMIM4
C 0.700 CausalMutation CLINVAR

dbSNP: rs876658517
rs876658517
ATM ; C11orf65
0.700 GeneticVariation UNIPROT

dbSNP: rs879255678
rs879255678
MPRIP ; FLCN
A 0.700 CausalMutation CLINVAR

dbSNP: rs35073794
rs35073794
TERC
0.010 GeneticVariation BEFREE (OR =1.52, 95% CI = 1.11-2.08, p = 0.009).<i>TERC</i>-rs35073794 was associated with an increased risk of RCC in the codominant model. 29100352

2017
dbSNP: rs1642742
rs1642742
VHL
0.010 GeneticVariation BEFREE rs1642742 and rs1642743 are candidate biomarkers for poor OS in m-ccRCC patients receiving first-line VEGFR-TKI. 29503246

2018
dbSNP: rs149617956
rs149617956
MITF
0.050 GeneticVariation BEFREE A French and an Australian study have recently identified a rare germline functional variant in the microphthalmia-associated transcription factor (MITF) (E318K) that predisposes to familial and sporadic melanoma and to renal cell carcinoma (RCC), showing a new link between two tumour types with different risk factors and between deregulated sumoylation and cancer. 23167872

2013
dbSNP: rs113488022
rs113488022
BRAF
0.010 GeneticVariation BEFREE A previous study identified BRAF V600E mutations in approximately 90% of MA and found that similar BRAF exon 15 mutations are exceedingly rare in other common renal tumors, including renal cell carcinoma and oncocytoma. 25602792

2015
dbSNP: rs121913377
rs121913377
BRAF
0.010 GeneticVariation BEFREE A previous study identified BRAF V600E mutations in approximately 90% of MA and found that similar BRAF exon 15 mutations are exceedingly rare in other common renal tumors, including renal cell carcinoma and oncocytoma. 25602792

2015
dbSNP: rs4765623
rs4765623
SCARB1
0.010 GeneticVariation BEFREE A recent genome-wide association study of renal cell carcinoma (RCC) in European population has identified genetic variants in the regions of 2p21 (rs7579899), 11q13.3 (rs7105934) and 12q24.31 (rs4765623) conferred susceptibility to RCC. 22131124

2012
dbSNP: rs1055259
rs1055259
GSTM3 ; GSTM5
0.010 GeneticVariation BEFREE A SNP-rs1055259 was found to be significantly associated with the susceptibility of ccRCC (OR = 0.59, 95% CI = 0.41-0.92; P = .019). 29569387

2018