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rs17781919

From SNPedia

Orientationplus
Make rs17781919(C;C)
Make rs17781919(C;T)
Make rs17781919(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position73276750
GeneNUMB
is asnp
is mentioned by
dbSNPrs17781919
ebirs17781919
HLIrs17781919
Exacrs17781919
Varsomers17781919
Maprs17781919
PheGenIrs17781919
hapmaprs17781919
1000 genomesrs17781919
hgdprs17781919
ensemblrs17781919
gopubmedrs17781919
geneviewrs17781919
scholarrs17781919
googlers17781919
pharmgkbrs17781919
gwascentralrs17781919
openSNPrs17781919
23andMers17781919
23andMe allrs17781919
SNP Nexus

SNPshotrs17781919
SNPdbers17781919
MSV3drs17781919
GWAS Ctlgrs17781919
Max Magnitude
? (C;C) (C;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