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rs12435797

From SNPedia

Orientationplus
Make rs12435797(G;G)
Make rs12435797(G;T)
Make rs12435797(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position73330961
GeneNUMB
is asnp
is mentioned by
dbSNPrs12435797
ebirs12435797
HLIrs12435797
Exacrs12435797
Varsomers12435797
Maprs12435797
PheGenIrs12435797
hapmaprs12435797
1000 genomesrs12435797
hgdprs12435797
ensemblrs12435797
gopubmedrs12435797
geneviewrs12435797
scholarrs12435797
googlers12435797
pharmgkbrs12435797
gwascentralrs12435797
openSNPrs12435797
23andMers12435797
23andMe allrs12435797
SNP Nexus

SNPshotrs12435797
SNPdbers12435797
MSV3drs12435797
GWAS Ctlgrs12435797
Max Magnitude
? (G;G) (G;T) (T;T) 28
[PMID 26264115OA-icon.png] Genetic variants of numb gene were associated with elevated total cholesterol level and low density lipoprotein cholesterol level in Chinese subjects, in Xinjiang, China

[PMID 26415596OA-icon.png] The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China