rs1019075
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1019075(A;A) |
Make rs1019075(A;G) |
Make rs1019075(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 73417339 |
Gene | NUMB |
is a | snp |
is | mentioned by |
dbSNP | rs1019075 |
dbSNP (classic) | rs1019075 |
ClinGen | rs1019075 |
ebi | rs1019075 |
HLI | rs1019075 |
Exac | rs1019075 |
Gnomad | rs1019075 |
Varsome | rs1019075 |
LitVar | rs1019075 |
Map | rs1019075 |
PheGenI | rs1019075 |
Biobank | rs1019075 |
1000 genomes | rs1019075 |
hgdp | rs1019075 |
ensembl | rs1019075 |
geneview | rs1019075 |
scholar | rs1019075 |
rs1019075 | |
pharmgkb | rs1019075 |
gwascentral | rs1019075 |
openSNP | rs1019075 |
23andMe | rs1019075 |
SNPshot | rs1019075 |
SNPdbe | rs1019075 |
MSV3d | rs1019075 |
GWAS Ctlg | rs1019075 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26264115] 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 26415596] The association of cholesterol absorption gene Numb polymorphism with Coronary Artery Disease among Han Chinese and Uighur Chinese in Xinjiang, China