rs17880487
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs17880487(C;T) |
Make rs17880487(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 21 |
Position | 31668917 |
Gene | SOD1 |
is a | snp |
is | mentioned by |
dbSNP | rs17880487 |
dbSNP (classic) | rs17880487 |
ClinGen | rs17880487 |
ebi | rs17880487 |
HLI | rs17880487 |
Exac | rs17880487 |
Gnomad | rs17880487 |
Varsome | rs17880487 |
LitVar | rs17880487 |
Map | rs17880487 |
PheGenI | rs17880487 |
Biobank | rs17880487 |
1000 genomes | rs17880487 |
hgdp | rs17880487 |
ensembl | rs17880487 |
geneview | rs17880487 |
scholar | rs17880487 |
rs17880487 | |
pharmgkb | rs17880487 |
gwascentral | rs17880487 |
openSNP | rs17880487 |
23andMe | rs17880487 |
SNPshot | rs17880487 |
SNPdbe | rs17880487 |
MSV3d | rs17880487 |
GWAS Ctlg | rs17880487 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 27755600] The Impact of Superoxide Dismutase-1 Genetic Variation on Cardiovascular and All-Cause Mortality in a Prospective Cohort Study: The Yamagata (Takahata) Study.
ClinVar | |
---|---|
Risk | rs17880487(T;T) |
Alt | rs17880487(T;T) |
Reference | Rs17880487(C;C) |
Significance | Probable-non-pathogenic |
Disease | Amyotrophic Lateral Sclerosis |
Variation | info |
Gene | SOD1 |
CLNDBN | Amyotrophic Lateral Sclerosis, Dominant |
Reversed | 0 |
HGVS | NC_000021.8:g.33041230C>T |
CLNSRC | |
CLNACC | RCV000407681.1, |