|
| Entrez Id: |
51230 |
| Gene Symbol: |
PHF20 |
PHF20
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Common sequence variants on 20q11.22 confer melanoma susceptibility.
|
18488026 |
2008 |
|
| Entrez Id: |
172 |
| Gene Symbol: |
AFG3L1P |
AFG3L1P
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.
|
21706340 |
2012 |
|
| Entrez Id: |
130540 |
| Gene Symbol: |
FLACC1 |
FLACC1
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies three new melanoma susceptibility loci.
|
21983787 |
2011 |
|
| Entrez Id: |
172 |
| Gene Symbol: |
AFG3L1P |
AFG3L1P
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies three loci associated with melanoma risk.
|
19578364 |
2009 |
|
| Entrez Id: |
128861 |
| Gene Symbol: |
BPIFA3 |
BPIFA3
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Common sequence variants on 20q11.22 confer melanoma susceptibility.
|
18488026 |
2008 |
|
| Entrez Id: |
8558 |
| Gene Symbol: |
CDK10 |
CDK10
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Identification of a melanoma susceptibility locus and somatic mutation in TET2.
|
24980573 |
2014 |
|
| Entrez Id: |
128861 |
| Gene Symbol: |
BPIFA3 |
BPIFA3
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies three new melanoma susceptibility loci.
|
21983787 |
2011 |
|
| Entrez Id: |
29123 |
| Gene Symbol: |
ANKRD11 |
ANKRD11
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.
|
21706340 |
2012 |
|
| Entrez Id: |
100996521 |
| Gene Symbol: |
CTXND2 |
CTXND2
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21.3.
|
21983785 |
2011 |
|
| Entrez Id: |
8558 |
| Gene Symbol: |
CDK10 |
CDK10
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies three loci associated with melanoma risk.
|
19578364 |
2009 |
|
| Entrez Id: |
54849 |
| Gene Symbol: |
DEF8 |
DEF8
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
|
21926416 |
2011 |
|
| Entrez Id: |
79007 |
| Gene Symbol: |
DBNDD1 |
DBNDD1
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.
|
21706340 |
2012 |
|
| Entrez Id: |
8558 |
| Gene Symbol: |
CDK10 |
CDK10
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
|
21926416 |
2011 |
|
| Entrez Id: |
8558 |
| Gene Symbol: |
CDK10 |
CDK10
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies three new melanoma susceptibility loci.
|
21983787 |
2011 |
|
| Entrez Id: |
79007 |
| Gene Symbol: |
DBNDD1 |
DBNDD1
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
|
21926416 |
2011 |
|
| Entrez Id: |
402359 |
| Gene Symbol: |
KHSRPP1 |
KHSRPP1
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
|
21926416 |
2011 |
|
| Entrez Id: |
8558 |
| Gene Symbol: |
CDK10 |
CDK10
|
0.100 |
GeneticVariation
|
disease |
GWASDB |
A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.
|
21706340 |
2012 |
|
| Entrez Id: |
5728 |
| Gene Symbol: |
PTEN |
PTEN
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Germline mutation of the tumour suppressor PTEN in Proteus syndrome.
|
12471211 |
2002 |
|
| Entrez Id: |
5728 |
| Gene Symbol: |
PTEN |
PTEN
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Germline mutations of the PTEN gene in Cowden disease, an inherited breast and thyroid cancer syndrome.
|
9140396 |
1997 |
|
| Entrez Id: |
5728 |
| Gene Symbol: |
PTEN |
PTEN
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
1029 |
| Gene Symbol: |
CDKN2A |
CDKN2A
|
0.800 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
1019 |
| Gene Symbol: |
CDK4 |
CDK4
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
7015 |
| Gene Symbol: |
TERT |
TERT
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
Expanding the clinical phenotype of autosomal dominant dyskeratosis congenita caused by TERT mutations.
|
18460650 |
2008 |
|
| Entrez Id: |
7015 |
| Gene Symbol: |
TERT |
TERT
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|
|
| Entrez Id: |
8314 |
| Gene Symbol: |
BAP1 |
BAP1
|
0.700 |
Biomarker
|
disease |
GENOMICS_ENGLAND |
|
|
|