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rs10483853

From SNPedia

Orientationminus
Stabilizedminus
Make rs10483853(C;C)
Make rs10483853(C;T)
Make rs10483853(T;T)
ReferenceGRCh38 38.1/141
Chromosome14
Position73289591
GeneNUMB
is asnp
is mentioned by
dbSNPrs10483853
ebirs10483853
HLIrs10483853
Exacrs10483853
Varsomers10483853
Maprs10483853
PheGenIrs10483853
hapmaprs10483853
1000 genomesrs10483853
hgdprs10483853
ensemblrs10483853
gopubmedrs10483853
geneviewrs10483853
scholarrs10483853
googlers10483853
pharmgkbrs10483853
gwascentralrs10483853
openSNPrs10483853
23andMers10483853
23andMe allrs10483853
SNP Nexus

SNPshotrs10483853
SNPdbers10483853
MSV3drs10483853
GWAS Ctlgrs10483853
GMAF0.3545
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs10483853
PubMedID [PMID 17903303OA-icon.png]
Condition Coronary artery calcification
Gene NUMB
Risk Allele
pValue 6.00E-006
OR NA
95% CI



GET Evidence
rs10483853
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.367188
summary