rs31271969
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs31271969(G;G) |
Make rs31271969(G;T) |
Make rs31271969(T;T) |
Reference | GRCm38 38.1/137 |
Chromosome | 15 |
Position | 68822600 |
is a | snp |
is | mentioned by |
dbSNP | rs31271969 |
dbSNP (classic) | rs31271969 |
ClinGen | rs31271969 |
ebi | rs31271969 |
HLI | rs31271969 |
Exac | rs31271969 |
Gnomad | rs31271969 |
Varsome | rs31271969 |
LitVar | rs31271969 |
Map | rs31271969 |
PheGenI | rs31271969 |
Biobank | rs31271969 |
1000 genomes | rs31271969 |
hgdp | rs31271969 |
ensembl | rs31271969 |
geneview | rs31271969 |
scholar | rs31271969 |
rs31271969 | |
pharmgkb | rs31271969 |
gwascentral | rs31271969 |
openSNP | rs31271969 |
23andMe | rs31271969 |
SNPshot | rs31271969 |
SNPdbe | rs31271969 |
MSV3d | rs31271969 |
GWAS Ctlg | rs31271969 |
Max Magnitude | 0 |
[PMID 20571108] Confirmation of Multiple Seizure Susceptibility QTLs on Chromosome 15 in C57BL/6J and DBA/2J Inbred Mice