rs431905516
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 3 | Carrier of an infantile Parkinsonism-dystonia mutation |
(T;T) | 8 | Infantile Parkinsonism-dystonia |
Reference | GRCh38 38.1/142 |
Chromosome | 5 |
Position | 1406226 |
Gene | SLC6A3 |
is a | snp |
is | mentioned by |
dbSNP | rs431905516 |
dbSNP (classic) | rs431905516 |
ClinGen | rs431905516 |
ebi | rs431905516 |
HLI | rs431905516 |
Exac | rs431905516 |
Gnomad | rs431905516 |
Varsome | rs431905516 |
LitVar | rs431905516 |
Map | rs431905516 |
PheGenI | rs431905516 |
Biobank | rs431905516 |
1000 genomes | rs431905516 |
hgdp | rs431905516 |
ensembl | rs431905516 |
geneview | rs431905516 |
scholar | rs431905516 |
rs431905516 | |
pharmgkb | rs431905516 |
gwascentral | rs431905516 |
openSNP | rs431905516 |
23andMe | rs431905516 |
SNPshot | rs431905516 |
SNPdbe | rs431905516 |
MSV3d | rs431905516 |
GWAS Ctlg | rs431905516 |
Max Magnitude | 8 |
c.1561C>T (p.Arg521Trp)
ClinVar | |
---|---|
Risk | Rs431905516(T;T) |
Alt | Rs431905516(T;T) |
Reference | Rs431905516(C;C) |
Significance | Pathogenic |
Disease | Infantile Parkinsonism-dystonia |
Variation | info |
Gene | SLC6A3 |
CLNDBN | Infantile Parkinsonism-dystonia |
Reversed | 1 |
HGVS | NC_000005.9:g.1406341G>A |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000083264.4, |