rs201096554
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs201096554(C;T) |
Make rs201096554(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 16 |
Position | 89530785 |
Gene | SPG7 |
is a | snp |
is | mentioned by |
dbSNP | rs201096554 |
dbSNP (classic) | rs201096554 |
ClinGen | rs201096554 |
ebi | rs201096554 |
HLI | rs201096554 |
Exac | rs201096554 |
Gnomad | rs201096554 |
Varsome | rs201096554 |
LitVar | rs201096554 |
Map | rs201096554 |
PheGenI | rs201096554 |
Biobank | rs201096554 |
1000 genomes | rs201096554 |
hgdp | rs201096554 |
ensembl | rs201096554 |
geneview | rs201096554 |
scholar | rs201096554 |
rs201096554 | |
pharmgkb | rs201096554 |
gwascentral | rs201096554 |
openSNP | rs201096554 |
23andMe | rs201096554 |
SNPshot | rs201096554 |
SNPdbe | rs201096554 |
MSV3d | rs201096554 |
GWAS Ctlg | rs201096554 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs201096554(T;T) |
Alt | rs201096554(T;T) |
Reference | Rs201096554(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | SPG7 |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000016.9:g.89597193C>T |
CLNSRC | |
CLNACC | RCV000198540.1, |