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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
ebirs10489849
HLIrs10489849
Exacrs10489849
Varsomers10489849
Maprs10489849
PheGenIrs10489849
hapmaprs10489849
1000 genomesrs10489849
hgdprs10489849
ensemblrs10489849
gopubmedrs10489849
geneviewrs10489849
scholarrs10489849
googlers10489849
pharmgkbrs10489849
gwascentralrs10489849
openSNPrs10489849
23andMers10489849
23andMe allrs10489849
SNP Nexus

SNPshotrs10489849
SNPdbers10489849
MSV3drs10489849
GWAS Ctlgrs10489849
GMAF0.2713
Max Magnitude
? (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


GET Evidence
rs10489849
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.289062
summary