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rs1019075

From SNPedia

Orientationminus
Make rs1019075(A;A)
Make rs1019075(A;G)
Make rs1019075(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position73417339
GeneNUMB
is asnp
is mentioned by
dbSNPrs1019075
ebirs1019075
HLIrs1019075
Exacrs1019075
Varsomers1019075
Maprs1019075
PheGenIrs1019075
hapmaprs1019075
1000 genomesrs1019075
hgdprs1019075
ensemblrs1019075
gopubmedrs1019075
geneviewrs1019075
scholarrs1019075
googlers1019075
pharmgkbrs1019075
gwascentralrs1019075
openSNPrs1019075
23andMers1019075
23andMe allrs1019075
SNP Nexus

SNPshotrs1019075
SNPdbers1019075
MSV3drs1019075
GWAS Ctlgrs1019075
Max Magnitude
? (A;A) (A;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