rs12435797
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12435797(G;G) |
Make rs12435797(G;T) |
Make rs12435797(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 14 |
Position | 73330961 |
Gene | NUMB |
is a | snp |
is | mentioned by |
dbSNP | rs12435797 |
dbSNP (classic) | rs12435797 |
ClinGen | rs12435797 |
ebi | rs12435797 |
HLI | rs12435797 |
Exac | rs12435797 |
Gnomad | rs12435797 |
Varsome | rs12435797 |
LitVar | rs12435797 |
Map | rs12435797 |
PheGenI | rs12435797 |
Biobank | rs12435797 |
1000 genomes | rs12435797 |
hgdp | rs12435797 |
ensembl | rs12435797 |
geneview | rs12435797 |
scholar | rs12435797 |
rs12435797 | |
pharmgkb | rs12435797 |
gwascentral | rs12435797 |
openSNP | rs12435797 |
23andMe | rs12435797 |
SNPshot | rs12435797 |
SNPdbe | rs12435797 |
MSV3d | rs12435797 |
GWAS Ctlg | rs12435797 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 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