rs13482630
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs13482630(C;C) |
Make rs13482630(C;T) |
Make rs13482630(T;T) |
Reference | GRCm38 38.1/137 |
Chromosome | 15 |
Position | 68492593 |
is a | snp |
is | mentioned by |
dbSNP | rs13482630 |
dbSNP (classic) | rs13482630 |
ClinGen | rs13482630 |
ebi | rs13482630 |
HLI | rs13482630 |
Exac | rs13482630 |
Gnomad | rs13482630 |
Varsome | rs13482630 |
LitVar | rs13482630 |
Map | rs13482630 |
PheGenI | rs13482630 |
Biobank | rs13482630 |
1000 genomes | rs13482630 |
hgdp | rs13482630 |
ensembl | rs13482630 |
geneview | rs13482630 |
scholar | rs13482630 |
rs13482630 | |
pharmgkb | rs13482630 |
gwascentral | rs13482630 |
openSNP | rs13482630 |
23andMe | rs13482630 |
SNPshot | rs13482630 |
SNPdbe | rs13482630 |
MSV3d | rs13482630 |
GWAS Ctlg | rs13482630 |
Max Magnitude | 0 |
[PMID 20571108] Confirmation of Multiple Seizure Susceptibility QTLs on Chromosome 15 in C57BL/6J and DBA/2J Inbred Mice