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rs13482630

From SNPedia

Orientationplus
Stabilizedplus
Make rs13482630(C;C)
Make rs13482630(C;T)
Make rs13482630(T;T)
ReferenceGRCm38 38.1/137
Chromosome15
Position68492593
is asnp
is mentioned by
dbSNPrs13482630
ebirs13482630
HLIrs13482630
Exacrs13482630
Varsomers13482630
Maprs13482630
PheGenIrs13482630
hapmaprs13482630
1000 genomesrs13482630
hgdprs13482630
ensemblrs13482630
gopubmedrs13482630
geneviewrs13482630
scholarrs13482630
googlers13482630
pharmgkbrs13482630
gwascentralrs13482630
openSNPrs13482630
23andMers13482630
23andMe allrs13482630
SNP Nexus

SNPshotrs13482630
SNPdbers13482630
MSV3drs13482630
GWAS Ctlgrs13482630
Max Magnitude

[PMID 20571108OA-icon.png] Confirmation of Multiple Seizure Susceptibility QTLs on Chromosome 15 in C57BL/6J and DBA/2J Inbred Mice