rs3761472
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs3761472(A;A) |
Make rs3761472(A;G) |
Make rs3761472(G;G) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 22 |
Position | 43972242 |
Gene | SAMM50 |
is a | snp |
is | mentioned by |
dbSNP | rs3761472 |
dbSNP (classic) | rs3761472 |
ClinGen | rs3761472 |
ebi | rs3761472 |
HLI | rs3761472 |
Exac | rs3761472 |
Gnomad | rs3761472 |
Varsome | rs3761472 |
LitVar | rs3761472 |
Map | rs3761472 |
PheGenI | rs3761472 |
Biobank | rs3761472 |
1000 genomes | rs3761472 |
hgdp | rs3761472 |
ensembl | rs3761472 |
geneview | rs3761472 |
scholar | rs3761472 |
rs3761472 | |
pharmgkb | rs3761472 |
gwascentral | rs3761472 |
openSNP | rs3761472 |
23andMe | rs3761472 |
SNPshot | rs3761472 |
SNPdbe | rs3761472 |
MSV3d | rs3761472 |
GWAS Ctlg | rs3761472 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 26587038] Genetic Variants in the SAMM50 Gene Create Susceptibility to Nonalcoholic Fatty Liver Disease in a Chinese Han Population