rs10513026
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in complete genomics |
Make rs10513026(A;A) |
Make rs10513026(A;C) |
Reference | GRCh38 38.1/141 |
Chromosome | 5 |
Position | 9623994 |
is a | snp |
is | mentioned by |
dbSNP | rs10513026 |
dbSNP (classic) | rs10513026 |
ClinGen | rs10513026 |
ebi | rs10513026 |
HLI | rs10513026 |
Exac | rs10513026 |
Gnomad | rs10513026 |
Varsome | rs10513026 |
LitVar | rs10513026 |
Map | rs10513026 |
PheGenI | rs10513026 |
Biobank | rs10513026 |
1000 genomes | rs10513026 |
hgdp | rs10513026 |
ensembl | rs10513026 |
geneview | rs10513026 |
scholar | rs10513026 |
rs10513026 | |
pharmgkb | rs10513026 |
gwascentral | rs10513026 |
openSNP | rs10513026 |
23andMe | rs10513026 |
SNPshot | rs10513026 |
SNPdbe | rs10513026 |
MSV3d | rs10513026 |
GWAS Ctlg | rs10513026 |
GMAF | 0.04086 |
Max Magnitude | 0 |
? | (A;A) (A;C) (C;C) | 28 |
---|---|---|
|
[PMID 19812673] A genome-wide linkage and association scan reveals novel loci for autism.