rs12541
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs12541(A;A) |
Make rs12541(A;G) |
Make rs12541(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 11 |
Position | 124753596 |
Gene | ESAM, VSIG2 |
is a | snp |
is | mentioned by |
dbSNP | rs12541 |
dbSNP (classic) | rs12541 |
ClinGen | rs12541 |
ebi | rs12541 |
HLI | rs12541 |
Exac | rs12541 |
Gnomad | rs12541 |
Varsome | rs12541 |
LitVar | rs12541 |
Map | rs12541 |
PheGenI | rs12541 |
Biobank | rs12541 |
1000 genomes | rs12541 |
hgdp | rs12541 |
ensembl | rs12541 |
geneview | rs12541 |
scholar | rs12541 |
rs12541 | |
pharmgkb | rs12541 |
gwascentral | rs12541 |
openSNP | rs12541 |
23andMe | rs12541 |
SNPshot | rs12541 |
SNPdbe | rs12541 |
MSV3d | rs12541 |
GWAS Ctlg | rs12541 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
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[PMID 24098564] The impact of genome-wide supported schizophrenia risk variants in the neurogranin gene on brain structure and function