rs1338041
From SNPedia
Orientation | minus |
Stabilized | minus |
Make rs1338041(G;G) |
Make rs1338041(G;T) |
Make rs1338041(T;T) |
Reference | GRCh38.p2 38.2/144 |
Chromosome | 13 |
Position | 101406511 |
Gene | NALCN |
is a | snp |
is | mentioned by |
dbSNP | rs1338041 |
dbSNP (classic) | rs1338041 |
ClinGen | rs1338041 |
ebi | rs1338041 |
HLI | rs1338041 |
Exac | rs1338041 |
Gnomad | rs1338041 |
Varsome | rs1338041 |
LitVar | rs1338041 |
Map | rs1338041 |
PheGenI | rs1338041 |
Biobank | rs1338041 |
1000 genomes | rs1338041 |
hgdp | rs1338041 |
ensembl | rs1338041 |
geneview | rs1338041 |
scholar | rs1338041 |
rs1338041 | |
pharmgkb | rs1338041 |
gwascentral | rs1338041 |
openSNP | rs1338041 |
23andMe | rs1338041 |
SNPshot | rs1338041 |
SNPdbe | rs1338041 |
MSV3d | rs1338041 |
GWAS Ctlg | rs1338041 |
Max Magnitude | 0 |
? | (G;G) (G;T) (T;T) | 28 |
---|---|---|
|
[PMID 25256078] Lack of validation of variants associated with cervical dystonia risk: a GWAS replication study