rs3914502
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs3914502(A;A) |
Make rs3914502(A;T) |
Make rs3914502(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 3 |
Position | 174846812 |
Gene | NAALADL2 |
is a | snp |
is | mentioned by |
dbSNP | rs3914502 |
dbSNP (classic) | rs3914502 |
ClinGen | rs3914502 |
ebi | rs3914502 |
HLI | rs3914502 |
Exac | rs3914502 |
Gnomad | rs3914502 |
Varsome | rs3914502 |
LitVar | rs3914502 |
Map | rs3914502 |
PheGenI | rs3914502 |
Biobank | rs3914502 |
1000 genomes | rs3914502 |
hgdp | rs3914502 |
ensembl | rs3914502 |
geneview | rs3914502 |
scholar | rs3914502 |
rs3914502 | |
pharmgkb | rs3914502 |
gwascentral | rs3914502 |
openSNP | rs3914502 |
23andMe | rs3914502 |
SNPshot | rs3914502 |
SNPdbe | rs3914502 |
MSV3d | rs3914502 |
GWAS Ctlg | rs3914502 |
Max Magnitude | 0 |
? | (A;A) (A;T) (T;T) | 28 |
---|---|---|
|
[PMID 26398136] Genome-Wide Association Study for Autism Spectrum Disorder in Taiwanese Han Population