rs35678
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs35678(C;C) |
Make rs35678(C;T) |
Make rs35678(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 10338239 |
Gene | ATP2B2 |
is a | snp |
is | mentioned by |
dbSNP | rs35678 |
dbSNP (classic) | rs35678 |
ClinGen | rs35678 |
ebi | rs35678 |
HLI | rs35678 |
Exac | rs35678 |
Gnomad | rs35678 |
Varsome | rs35678 |
LitVar | rs35678 |
Map | rs35678 |
PheGenI | rs35678 |
Biobank | rs35678 |
1000 genomes | rs35678 |
hgdp | rs35678 |
ensembl | rs35678 |
geneview | rs35678 |
scholar | rs35678 |
rs35678 | |
pharmgkb | rs35678 |
gwascentral | rs35678 |
openSNP | rs35678 |
23andMe | rs35678 |
SNPshot | rs35678 |
SNPdbe | rs35678 |
MSV3d | rs35678 |
GWAS Ctlg | rs35678 |
GMAF | 0.4734 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 22739633] The association of rs4307059 and rs35678 markers with autism spectrum disorders is replicated in Italian families
[PMID 20678243] Assessing the impact of a combined analysis of four common low-risk genetic variants on autism risk.