rs864309483
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
(C;T) | 6 | Dyskinesia, familial, with facial myokymia |
Make rs864309483(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 3 |
Position | 123352464 |
Gene | ADCY5 |
is a | snp |
is | mentioned by |
dbSNP | rs864309483 |
dbSNP (classic) | rs864309483 |
ClinGen | rs864309483 |
ebi | rs864309483 |
HLI | rs864309483 |
Exac | rs864309483 |
Gnomad | rs864309483 |
Varsome | rs864309483 |
LitVar | rs864309483 |
Map | rs864309483 |
PheGenI | rs864309483 |
Biobank | rs864309483 |
1000 genomes | rs864309483 |
hgdp | rs864309483 |
ensembl | rs864309483 |
geneview | rs864309483 |
scholar | rs864309483 |
rs864309483 | |
pharmgkb | rs864309483 |
gwascentral | rs864309483 |
openSNP | rs864309483 |
23andMe | rs864309483 |
SNPshot | rs864309483 |
SNPdbe | rs864309483 |
MSV3d | rs864309483 |
GWAS Ctlg | rs864309483 |
Max Magnitude | 6 |
aka c.1252C>T (p.Arg418Trp or R418W)
considered "definitely pathogenic" in the Movement Disorder Society Genetic mutation database (MDSGene) for autosomal dominant familial dyskinesia, with facial myokymia
see also OMIM 600293.0002
ClinVar | |
---|---|
Risk | rs864309483(T;T) |
Alt | rs864309483(T;T) |
Reference | Rs864309483(C;C) |
Significance | Pathogenic |
Disease | Dyskinesia not provided |
Variation | info |
Gene | ADCY5 |
CLNDBN | Dyskinesia, familial, with facial myokymia not provided |
Reversed | 1 |
HGVS | NC_000003.11:g.123071311G>A |
CLNSRC | OMIM Allelic Variant UniProtKB (protein) |
CLNACC | RCV000202545.2, RCV000255111.1, |