rs13036957
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in complete genomics |
Make rs13036957(A;A) |
Make rs13036957(A;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 20 |
Position | 43193056 |
is a | snp |
is | mentioned by |
dbSNP | rs13036957 |
dbSNP (classic) | rs13036957 |
ClinGen | rs13036957 |
ebi | rs13036957 |
HLI | rs13036957 |
Exac | rs13036957 |
Gnomad | rs13036957 |
Varsome | rs13036957 |
LitVar | rs13036957 |
Map | rs13036957 |
PheGenI | rs13036957 |
Biobank | rs13036957 |
1000 genomes | rs13036957 |
hgdp | rs13036957 |
ensembl | rs13036957 |
geneview | rs13036957 |
scholar | rs13036957 |
rs13036957 | |
pharmgkb | rs13036957 |
gwascentral | rs13036957 |
openSNP | rs13036957 |
23andMe | rs13036957 |
SNPshot | rs13036957 |
SNPdbe | rs13036957 |
MSV3d | rs13036957 |
GWAS Ctlg | rs13036957 |
GMAF | 0.1956 |
Max Magnitude | 0 |
? | (A;A) (A;G) (G;G) | 28 |
---|---|---|
|
This SNP was associated with amyotrophic lateral sclerosis (ALS) based on a study of 1,152 patients.[PMID 17671248]