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rs7591996

From SNPedia

Orientationplus
Stabilizedplus
Make rs7591996(A;A)
Make rs7591996(A;C)
Make rs7591996(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position6321289
is asnp
is mentioned by
dbSNPrs7591996
dbSNP (classic)rs7591996
ClinGenrs7591996
ebirs7591996
HLIrs7591996
Exacrs7591996
Gnomadrs7591996
Varsomers7591996
LitVarrs7591996
Maprs7591996
PheGenIrs7591996
Biobankrs7591996
1000 genomesrs7591996
hgdprs7591996
ensemblrs7591996
geneviewrs7591996
scholarrs7591996
googlers7591996
pharmgkbrs7591996
gwascentralrs7591996
openSNPrs7591996
23andMers7591996
SNPshotrs7591996
SNPdbers7591996
MSV3drs7591996
GWAS Ctlgrs7591996
GMAF0.3765
Max Magnitude0
? (A;A) (A;C) (C;C) 28


GWAS snp
PMID [PMID 23727862OA-icon.png]
Trait Osteosarcoma
Title Genome-wide association study identifies two susceptibility loci for osteosarcoma.
Risk Allele C
P-val 1E-8
Odds Ratio 1.39 [1.23-1.54]