Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs587776576
rs587776576
WT1
T 0.700 CausalMutation CLINVAR Genetic screening in adolescents with steroid-resistant nephrotic syndrome. 23515051

2013
dbSNP: rs10060683
rs10060683 		0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs11913239
rs11913239
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR CHEK2*1100delC and risk of malignant melanoma: Danish and German studies and meta-analysis. 21956126

2012
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR CHEK2 1100delC variant and breast cancer risk in Caucasians: a meta-analysis based on 25 studies with 29,154 cases and 37,064 controls. 22994785

2012
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR A risk of essential thrombocythemia in carriers of constitutional CHEK2 gene mutations. 22058216

2012
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR Frequency of the CHEK2 1100delC mutation among women with early-onset and bilateral breast cancer. 22520019

2012
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR Breast carcinoma and Lynch syndrome: molecular analysis of tumors arising in mutation carriers, non-carriers, and sporadic cases. 22691310

2012
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR CHEK2*1100delC heterozygosity in women with breast cancer associated with early death, breast cancer-specific death, and increased risk of a second breast cancer. 23109706

2012
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR CHEK2 1100DELC germline mutation: a frequency study in hereditary breast and colon cancer Brazilian families. 23329222

2012
dbSNP: rs16988855
rs16988855
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs2009857
rs2009857
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs2221269
rs2221269
LOC105379082
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs2267166
rs2267166
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs61344503
rs61344503
LOC105379082
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs6887553
rs6887553 		0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs7288385
rs7288385
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs7288627
rs7288627
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs7290898
rs7290898
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs8141515
rs8141515
TCN2
0.700 GeneticVariation GWASDB A genome-wide association study identifies susceptibility loci for Wilms tumor. 22544364

2012
dbSNP: rs121907909
rs121907909
WT1
A 0.700 CausalMutation CLINVAR Clinical pictures and novel mutations of WT1-associated Denys-Drash syndrome in two Chinese children. 21851196

2011
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing. 22006311

2011
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR CHEK2*1100delC homozygosity is associated with a high breast cancer risk in women. 22058428

2011
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR Rare, evolutionarily unlikely missense substitutions in CHEK2 contribute to breast cancer susceptibility: results from a breast cancer family registry case-control mutation-screening study. 21244692

2011
dbSNP: rs1555913934
rs1555913934
CHEK2
C 0.700 CausalMutation CLINVAR Risk of breast cancer in women with a CHEK2 mutation with and without a family history of breast cancer. 21876083

2011