rs13097028
|
|
|
0.800 |
GeneticVariation |
GWASCAT |
Identification of a melanoma susceptibility locus and somatic mutation in TET2.
|
24980573 |
2014 |
rs13097028
|
|
|
0.800 |
GeneticVariation |
GWASDB |
Identification of a melanoma susceptibility locus and somatic mutation in TET2.
|
24980573 |
2014 |
rs4911414
|
|
|
0.710 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies three new melanoma susceptibility loci.
|
21983787 |
2011 |
rs4911414
|
|
|
0.710 |
GeneticVariation |
BEFREE |
Except for rs1015363, none of the 12 tagging SNPs, genotyped to cover 239.9 kb region with polymorphisms linked to rs4911414 and rs1015362, were associated with melanoma.
|
22628150 |
2013 |
rs11263498
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies three new melanoma susceptibility loci.
|
21983787 |
2011 |
rs1341866
|
|
|
0.700 |
GeneticVariation |
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 |
rs1485993
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies three new melanoma susceptibility loci.
|
21983787 |
2011 |
rs228437
|
|
G |
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies three new melanoma susceptibility loci.
|
21983787 |
2011 |
rs4785752
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
|
21926416 |
2011 |
rs498136
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.
|
28212542 |
2017 |
rs62389423
|
|
A |
0.700 |
GeneticVariation |
GWASCAT |
Two-stage genome-wide association study identifies a novel susceptibility locus associated with melanoma.
|
28212542 |
2017 |
rs7033503
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Genome-wide association study identifies novel loci predisposing to cutaneous melanoma.
|
21926416 |
2011 |
rs721970
|
|
|
0.700 |
GeneticVariation |
GWASDB |
Common sequence variants on 20q11.22 confer melanoma susceptibility.
|
18488026 |
2008 |
rs36115365
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Herein, we investigated the modifying capacities of rs36115365-C on PC and melanoma in a cohort of 283 p16-Leiden carriers including 29 diagnosed with PC, 171 diagnosed with melanoma, 21 diagnosed with both PC and melanoma and 62 with neither PC nor melanoma.
|
31203567 |
2019 |
rs36115365
|
|
|
0.020 |
GeneticVariation |
BEFREE |
Of these, rs36115365-C associated with increased pancreatic and testicular but decreased lung cancer and melanoma risk, and exhibited preferred protein-binding and enhanced regulatory activity.
|
28447668 |
2017 |
rs1015362
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Except for rs1015363, none of the 12 tagging SNPs, genotyped to cover 239.9 kb region with polymorphisms linked to rs4911414 and rs1015362, were associated with melanoma.
|
22628150 |
2013 |
rs1015363
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Except for rs1015363, none of the 12 tagging SNPs, genotyped to cover 239.9 kb region with polymorphisms linked to rs4911414 and rs1015362, were associated with melanoma.
|
22628150 |
2013 |
rs10816595
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Individuals having melanoma in a visibly UV-damaged site were more likely to carry MC1R rs75570604 (odds ratio [OR] 2.5), 9q31.2 rs10816595 (OR 2.5), and MTAP rs869329 (OR 1.4); these same alleles were more common in MPM patients diagnosed ≤40 years.
|
31794051 |
2019 |
rs12029406
|
|
|
0.010 |
GeneticVariation |
BEFREE |
In the melanoma dataset, two pancreatic cancer susceptibility variants were associated: NR5A2 (rs12029406; OR, 1.39; 95% CI, 1.01-1.92; P = 0.04) and CLPTM1L-TERT (rs401681; OR, 1.16; 95% CI, 1.01-1.34; P = 0.04).
|
24642353 |
2014 |
rs12512631
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We found association between SNP rs12512631, located 3'downstream of GC, and risk of CM that seems to fit a dominant model (OR 1.63 95%CI 1.23-2.17 p-value 7×10(-4)).
|
23544077 |
2013 |
rs2127675
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Two SNPs (rs1351383 and rs2127675) were associated with melanoma risk in the GenoMEL data set (P = 0.013 and 0.004, respectively), but failed in validation using the Australian data set.
|
23360169 |
2013 |
rs5759167
|
|
|
0.010 |
GeneticVariation |
BEFREE |
Among the probands, a significantly increased frequency of leukemia was found in the carriers of SNP rs2736098 (5p15, P = .03) and melanoma in the carriers of either SNP rs1512268 (8p21, P = .006) or SNP rs5759167 (22q13, P = .02).
|
21820706 |
2011 |
rs6673928
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We identified highly significant associations with better melanoma OS for rs6673928, impacting IL19 expression (HR, 0.56; 95% CI, 0.41-0.77; P = 0.0002) and rs6695772, controlling the expression of BATF3 (HR, 1.64; 95% CI, 1.19-2.24; P = 0.0019).
|
26733611 |
2016 |
rs6695772
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We identified highly significant associations with better melanoma OS for rs6673928, impacting IL19 expression (HR, 0.56; 95% CI, 0.41-0.77; P = 0.0002) and rs6695772, controlling the expression of BATF3 (HR, 1.64; 95% CI, 1.19-2.24; P = 0.0019).
|
26733611 |
2016 |
rs7335046
|
|
|
0.010 |
GeneticVariation |
BEFREE |
We further evaluated the associations of these two novel SNPs (rs12210050 and rs7335046) with squamous cell carcinoma (SCC) risk as well as melanoma risk.
|
21700618 |
2011 |