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rs13016963

From SNPedia

Orientationplus
Stabilizedplus
Make rs13016963(A;A)
Make rs13016963(A;G)
Make rs13016963(G;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position201298088
GeneALS2CR12
is asnp
is mentioned by
dbSNPrs13016963
ebirs13016963
HLIrs13016963
Exacrs13016963
Varsomers13016963
Maprs13016963
PheGenIrs13016963
hapmaprs13016963
1000 genomesrs13016963
hgdprs13016963
ensemblrs13016963
gopubmedrs13016963
geneviewrs13016963
scholarrs13016963
googlers13016963
pharmgkbrs13016963
gwascentralrs13016963
openSNPrs13016963
23andMers13016963
23andMe allrs13016963
SNP Nexus

SNPshotrs13016963
SNPdbers13016963
MSV3drs13016963
GWAS Ctlgrs13016963
GMAF0.4027
Max Magnitude
? (A;A) (A;G) (G;G) 28
[PMID 22323360OA-icon.png] Genotypic variants at 2q33 and risk of esophageal squamous cell carcinoma in China: A meta-analysis of genome-wide association studies
GWAS snp
PMID [PMID 21983787OA-icon.png]
Trait
Title Genome-wide association study identifies three new melanoma susceptibility loci.
Risk Allele A
P-val 9E-10
Odds Ratio 1.1400 None


[PMID 26635288] Pathway, in silico and tissue-specific expression quantitative analyses of oesophageal squamous cell carcinoma genome-wide association studies data.