rs797044595
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs797044595(G;G) |
Make rs797044595(G;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 1 |
Position | 11022562 |
Gene | TARDBP |
is a | snp |
is | mentioned by |
dbSNP | rs797044595 |
dbSNP (classic) | rs797044595 |
ClinGen | rs797044595 |
ebi | rs797044595 |
HLI | rs797044595 |
Exac | rs797044595 |
Gnomad | rs797044595 |
Varsome | rs797044595 |
LitVar | rs797044595 |
Map | rs797044595 |
PheGenI | rs797044595 |
Biobank | rs797044595 |
1000 genomes | rs797044595 |
hgdp | rs797044595 |
ensembl | rs797044595 |
geneview | rs797044595 |
scholar | rs797044595 |
rs797044595 | |
pharmgkb | rs797044595 |
gwascentral | rs797044595 |
openSNP | rs797044595 |
23andMe | rs797044595 |
SNPshot | rs797044595 |
SNPdbe | rs797044595 |
MSV3d | rs797044595 |
GWAS Ctlg | rs797044595 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs797044595(G;G) |
Alt | rs797044595(G;G) |
Reference | Rs797044595(T;T) |
Significance | Pathogenic |
Disease | Amyotrophic lateral sclerosis type 10 |
Variation | info |
Gene | TARDBP |
CLNDBN | Amyotrophic lateral sclerosis type 10 |
Reversed | 0 |
HGVS | NC_000001.10:g.11082619T>G |
CLNSRC | |
CLNACC | RCV000192196.1, |