rs12740310
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 |
Make rs12740310(C;T) |
Make rs12740310(T;T) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 220589182 |
Gene | MARK1 |
is a | snp |
is | mentioned by |
dbSNP | rs12740310 |
dbSNP (classic) | rs12740310 |
ClinGen | rs12740310 |
ebi | rs12740310 |
HLI | rs12740310 |
Exac | rs12740310 |
Gnomad | rs12740310 |
Varsome | rs12740310 |
LitVar | rs12740310 |
Map | rs12740310 |
PheGenI | rs12740310 |
Biobank | rs12740310 |
1000 genomes | rs12740310 |
hgdp | rs12740310 |
ensembl | rs12740310 |
geneview | rs12740310 |
scholar | rs12740310 |
rs12740310 | |
pharmgkb | rs12740310 |
gwascentral | rs12740310 |
openSNP | rs12740310 |
23andMe | rs12740310 |
SNPshot | rs12740310 |
SNPdbe | rs12740310 |
MSV3d | rs12740310 |
GWAS Ctlg | rs12740310 |
GMAF | 0.03903 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 18492799] Haplotype rs12740310*C-rs3737296*G-rs12410279*A was overtransmitted (p(corrected)=0.0016), with a relative risk for autism of 1.8 in homozygous carriers