Rs10871290

From SNPedia
Jump to: navigation, search

Orientationplus
Make rs10871290(C;C)
Make rs10871290(C;T)
Make rs10871290(T;T)
ReferenceGRCh38 38.1/141
Chromosome16
Position74438798
is asnp
is mentioned by
dbSNPrs10871290
PheGenIrs10871290
nextbiors10871290
hapmaprs10871290
1000 genomesrs10871290
hgdprs10871290
ensemblrs10871290
gopubmedrs10871290
geneviewrs10871290
scholarrs10871290
googlers10871290
pharmgkbrs10871290
gwascentralrs10871290
openSNPrs10871290
23andMers10871290
23andMe allrs10871290
SNP Nexus

SNPshotrs10871290
SNPdbers10871290
MSV3drs10871290
GMAF0.3756
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS
SNP rs10871290
PubMedID [PMID 18463975]
Condition Breast cancer
Gene GLG1
Risk Allele
pValue 4.00E-007
OR NA
95% CI



GET Evidence
rs10871290
aa_change
aa_change_short
impact pathogenic
qualified_impact Insufficiently evaluated pathogenic
overall_frequency 0.625
summary