rs80356725
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(A;A) | 0 | common in clinvar |
Make rs80356725(A;G) |
Make rs80356725(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 1 |
Position | 11022340 |
Gene | TARDBP |
is a | snp |
is | mentioned by |
dbSNP | rs80356725 |
dbSNP (classic) | rs80356725 |
ClinGen | rs80356725 |
ebi | rs80356725 |
HLI | rs80356725 |
Exac | rs80356725 |
Gnomad | rs80356725 |
Varsome | rs80356725 |
LitVar | rs80356725 |
Map | rs80356725 |
PheGenI | rs80356725 |
Biobank | rs80356725 |
1000 genomes | rs80356725 |
hgdp | rs80356725 |
ensembl | rs80356725 |
geneview | rs80356725 |
scholar | rs80356725 |
rs80356725 | |
pharmgkb | rs80356725 |
gwascentral | rs80356725 |
openSNP | rs80356725 |
23andMe | rs80356725 |
SNPshot | rs80356725 |
SNPdbe | rs80356725 |
MSV3d | rs80356725 |
GWAS Ctlg | rs80356725 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs80356725(G;G) |
Alt | rs80356725(G;G) |
Reference | Rs80356725(A;A) |
Significance | Pathogenic |
Disease | Amyotrophic lateral sclerosis type 10 |
Variation | info |
Gene | TARDBP |
CLNDBN | Amyotrophic lateral sclerosis type 10 |
Reversed | 0 |
HGVS | NC_000001.11:g.11022340A>G |
CLNSRC | ClinVar GeneReviews |
CLNACC | RCV000020676.1, |