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rs10476823

From SNPedia

Orientationplus
Stabilizedplus
Make rs10476823(C;C)
Make rs10476823(C;T)
Make rs10476823(T;T)
ReferenceGRCh38 38.1/142
Chromosome5
Position155434249
is asnp
is mentioned by
dbSNPrs10476823
ebirs10476823
HLIrs10476823
Exacrs10476823
Varsomers10476823
Maprs10476823
PheGenIrs10476823
hapmaprs10476823
1000 genomesrs10476823
hgdprs10476823
ensemblrs10476823
gopubmedrs10476823
geneviewrs10476823
scholarrs10476823
googlers10476823
pharmgkbrs10476823
gwascentralrs10476823
openSNPrs10476823
23andMers10476823
23andMe allrs10476823
SNP Nexus

SNPshotrs10476823
SNPdbers10476823
MSV3drs10476823
GWAS Ctlgrs10476823
Max Magnitude
? (C;C) (C;T) (T;T) 28

[PMID 24861865] Genetic variants in apoptosis-related genes associated with colorectal hyperplasia