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rs17119461

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common on affy axiom data
Make rs17119461(C;C)
Make rs17119461(C;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position105756594
GeneLOC101927549
is asnp
is mentioned by
dbSNPrs17119461
ebirs17119461
HLIrs17119461
Exacrs17119461
Varsomers17119461
Maprs17119461
PheGenIrs17119461
hapmaprs17119461
1000 genomesrs17119461
hgdprs17119461
ensemblrs17119461
gopubmedrs17119461
geneviewrs17119461
scholarrs17119461
googlers17119461
pharmgkbrs17119461
gwascentralrs17119461
openSNPrs17119461
23andMers17119461
23andMe allrs17119461
SNP Nexus

SNPshotrs17119461
SNPdbers17119461
MSV3drs17119461
GWAS Ctlgrs17119461
GMAF0.07117
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21706340]
Trait
Title A unique genome-wide association analysis in extended Utah high-risk pedigrees identifies a novel melanoma risk variant on chromosome arm 10q.
Risk Allele
P-val 7E-12
Odds Ratio 8.4000 [4.20-17.0]