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rs10484761

From SNPedia

Orientationminus
Stabilizedminus
Make rs10484761(A;A)
Make rs10484761(A;G)
Make rs10484761(G;G)
ReferenceGRCh38 38.1/141
Chromosome6
Position40834522
is asnp
is mentioned by
dbSNPrs10484761
ebirs10484761
HLIrs10484761
Exacrs10484761
Varsomers10484761
Maprs10484761
PheGenIrs10484761
hapmaprs10484761
1000 genomesrs10484761
hgdprs10484761
ensemblrs10484761
gopubmedrs10484761
geneviewrs10484761
scholarrs10484761
googlers10484761
pharmgkbrs10484761
gwascentralrs10484761
openSNPrs10484761
23andMers10484761
23andMe allrs10484761
SNP Nexus

SNPshotrs10484761
SNPdbers10484761
MSV3drs10484761
GWAS Ctlgrs10484761
GMAF0.258
Max Magnitude
? (A;A) (A;G) (G;G) 28
GWAS snp
PMID [PMID 21642993]
Trait
Title Genome-wide association study identifies three new susceptibility loci for esophageal squamous-cell carcinoma in Chinese populations.
Risk Allele G
P-val 7E-12
Odds Ratio 1.3300 [1.23-1.45]


[PMID 23151416] Genetic variants at 10q23 are associated with risk of head and neck cancer in a Chinese population


[PMID 24325909] Genetic variation rs10484761 on 6p21.1 derived from a genome-wide association study is associated with gastric cancer survival in a Chinese population