rs1009153
From SNPedia
Orientation | plus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common/normal in ClinVar |
Make rs1009153(C;T) |
Make rs1009153(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 15 |
Position | 22896157 |
Gene | CYFIP1 |
is a | snp |
is | mentioned by |
dbSNP | rs1009153 |
dbSNP (classic) | rs1009153 |
ClinGen | rs1009153 |
ebi | rs1009153 |
HLI | rs1009153 |
Exac | rs1009153 |
Gnomad | rs1009153 |
Varsome | rs1009153 |
LitVar | rs1009153 |
Map | rs1009153 |
PheGenI | rs1009153 |
Biobank | rs1009153 |
1000 genomes | rs1009153 |
hgdp | rs1009153 |
ensembl | rs1009153 |
geneview | rs1009153 |
scholar | rs1009153 |
rs1009153 | |
pharmgkb | rs1009153 |
gwascentral | rs1009153 |
openSNP | rs1009153 |
23andMe | rs1009153 |
SNPshot | rs1009153 |
SNPdbe | rs1009153 |
MSV3d | rs1009153 |
GWAS Ctlg | rs1009153 |
GMAF | 0.399 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22317777] Rare CNVs and Tag SNPs at 15q11.2 Are Associated With Schizophrenia in the Han Chinese Population