Have questions? Visit https://www.reddit.com/r/SNPedia

rs2108552

From SNPedia

Orientationminus
Make rs2108552(C;C)
Make rs2108552(C;G)
Make rs2108552(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position73410218
GeneNUMB
is asnp
is mentioned by
dbSNPrs2108552
ebirs2108552
HLIrs2108552
Exacrs2108552
Varsomers2108552
Maprs2108552
PheGenIrs2108552
hapmaprs2108552
1000 genomesrs2108552
hgdprs2108552
ensemblrs2108552
gopubmedrs2108552
geneviewrs2108552
scholarrs2108552
googlers2108552
pharmgkbrs2108552
gwascentralrs2108552
openSNPrs2108552
23andMers2108552
23andMe allrs2108552
SNP Nexus

SNPshotrs2108552
SNPdbers2108552
MSV3drs2108552
GWAS Ctlgrs2108552
Max Magnitude
? (C;C) (C;G) (G;G) 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