rs62037369
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs62037369(C;C) |
Make rs62037369(C;T) |
Make rs62037369(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 16 |
Position | 28872520 |
Gene | SH2B1 |
is a | snp |
is | mentioned by |
dbSNP | rs62037369 |
dbSNP (classic) | rs62037369 |
ClinGen | rs62037369 |
ebi | rs62037369 |
HLI | rs62037369 |
Exac | rs62037369 |
Gnomad | rs62037369 |
Varsome | rs62037369 |
LitVar | rs62037369 |
Map | rs62037369 |
PheGenI | rs62037369 |
Biobank | rs62037369 |
1000 genomes | rs62037369 |
hgdp | rs62037369 |
ensembl | rs62037369 |
geneview | rs62037369 |
scholar | rs62037369 |
rs62037369 | |
pharmgkb | rs62037369 |
gwascentral | rs62037369 |
openSNP | rs62037369 |
23andMe | rs62037369 |
SNPshot | rs62037369 |
SNPdbe | rs62037369 |
MSV3d | rs62037369 |
GWAS Ctlg | rs62037369 |
GMAF | 0.2176 |
Max Magnitude | 0 |
[PMID 23270367] Mutation screen in the GWAS derived obesity gene SH2B1 including functional analyses of detected variants