rs4327572
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs4327572(C;C) |
Make rs4327572(C;T) |
Make rs4327572(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 25972712 |
is a | snp |
is | mentioned by |
dbSNP | rs4327572 |
dbSNP (classic) | rs4327572 |
ClinGen | rs4327572 |
ebi | rs4327572 |
HLI | rs4327572 |
Exac | rs4327572 |
Gnomad | rs4327572 |
Varsome | rs4327572 |
LitVar | rs4327572 |
Map | rs4327572 |
PheGenI | rs4327572 |
Biobank | rs4327572 |
1000 genomes | rs4327572 |
hgdp | rs4327572 |
ensembl | rs4327572 |
geneview | rs4327572 |
scholar | rs4327572 |
rs4327572 | |
pharmgkb | rs4327572 |
gwascentral | rs4327572 |
openSNP | rs4327572 |
23andMe | rs4327572 |
SNPshot | rs4327572 |
SNPdbe | rs4327572 |
MSV3d | rs4327572 |
GWAS Ctlg | rs4327572 |
GMAF | 0.2397 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 19456320] A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.