rs12518194
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs12518194(A;A) |
Make rs12518194(A;G) |
Make rs12518194(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 25951452 |
is a | snp |
is | mentioned by |
dbSNP | rs12518194 |
dbSNP (classic) | rs12518194 |
ClinGen | rs12518194 |
ebi | rs12518194 |
HLI | rs12518194 |
Exac | rs12518194 |
Gnomad | rs12518194 |
Varsome | rs12518194 |
LitVar | rs12518194 |
Map | rs12518194 |
PheGenI | rs12518194 |
Biobank | rs12518194 |
1000 genomes | rs12518194 |
hgdp | rs12518194 |
ensembl | rs12518194 |
geneview | rs12518194 |
scholar | rs12518194 |
rs12518194 | |
pharmgkb | rs12518194 |
gwascentral | rs12518194 |
openSNP | rs12518194 |
23andMe | rs12518194 |
SNPshot | rs12518194 |
SNPdbe | rs12518194 |
MSV3d | rs12518194 |
GWAS Ctlg | rs12518194 |
GMAF | 0.2369 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
[PMID 19456320] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.