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rs10489849

From SNPedia

Orientationplus
Stabilizedplus
Make rs10489849(C;C)
Make rs10489849(C;T)
Make rs10489849(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position159226975
is asnp
is mentioned by
dbSNPrs10489849
dbSNP (classic)rs10489849
ClinGenrs10489849
ebirs10489849
HLIrs10489849
Exacrs10489849
Gnomadrs10489849
Varsomers10489849
LitVarrs10489849
Maprs10489849
PheGenIrs10489849
Biobankrs10489849
1000 genomesrs10489849
hgdprs10489849
ensemblrs10489849
geneviewrs10489849
scholarrs10489849
googlers10489849
pharmgkbrs10489849
gwascentralrs10489849
openSNPrs10489849
23andMers10489849
SNPshotrs10489849
SNPdbers10489849
MSV3drs10489849
GWAS Ctlgrs10489849
GMAF0.2713
Max Magnitude0
? (C;C) (C;T) (T;T) 28


GWAS snp
PMID [PMID 17903293OA-icon.png]
Trait Select biomarker traits
Title Genome-wide association with select biomarker traits in the Framingham Heart Study
Risk Allele
P-val 9.9999999999999995E-7
Odds Ratio NR NR