rs875989840
From SNPedia
Orientation | minus |
Stabilized | minus |
Geno | Mag | Summary |
---|---|---|
(T;T) | 0 | common in clinvar |
Make rs875989840(C;C) |
Make rs875989840(C;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 6 |
Position | 165416280 |
Gene | PDE10A |
is a | snp |
is | mentioned by |
dbSNP | rs875989840 |
dbSNP (classic) | rs875989840 |
ClinGen | rs875989840 |
ebi | rs875989840 |
HLI | rs875989840 |
Exac | rs875989840 |
Gnomad | rs875989840 |
Varsome | rs875989840 |
LitVar | rs875989840 |
Map | rs875989840 |
PheGenI | rs875989840 |
Biobank | rs875989840 |
1000 genomes | rs875989840 |
hgdp | rs875989840 |
ensembl | rs875989840 |
geneview | rs875989840 |
scholar | rs875989840 |
rs875989840 | |
pharmgkb | rs875989840 |
gwascentral | rs875989840 |
openSNP | rs875989840 |
23andMe | rs875989840 |
SNPshot | rs875989840 |
SNPdbe | rs875989840 |
MSV3d | rs875989840 |
GWAS Ctlg | rs875989840 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs875989840(C;C) |
Alt | rs875989840(C;C) |
Reference | Rs875989840(T;T) |
Significance | Pathogenic |
Disease | Striatal degeneration |
Variation | info |
Gene | PDE10A |
CLNDBN | Striatal degeneration, autosomal dominant 2 |
Reversed | 1 |
HGVS | NC_000006.11:g.165829768A>G |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000210938.1, |