rs864622781
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(G;G) | 0 | common in clinvar |
Make rs864622781(G;T) |
Make rs864622781(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 10 |
Position | 122488926 |
Gene | HTRA1, LOC105378526 |
is a | snp |
is | mentioned by |
dbSNP | rs864622781 |
dbSNP (classic) | rs864622781 |
ClinGen | rs864622781 |
ebi | rs864622781 |
HLI | rs864622781 |
Exac | rs864622781 |
Gnomad | rs864622781 |
Varsome | rs864622781 |
LitVar | rs864622781 |
Map | rs864622781 |
PheGenI | rs864622781 |
Biobank | rs864622781 |
1000 genomes | rs864622781 |
hgdp | rs864622781 |
ensembl | rs864622781 |
geneview | rs864622781 |
scholar | rs864622781 |
rs864622781 | |
pharmgkb | rs864622781 |
gwascentral | rs864622781 |
openSNP | rs864622781 |
23andMe | rs864622781 |
SNPshot | rs864622781 |
SNPdbe | rs864622781 |
MSV3d | rs864622781 |
GWAS Ctlg | rs864622781 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs864622781(T;T) |
Alt | rs864622781(T;T) |
Reference | Rs864622781(G;G) |
Significance | Pathogenic |
Disease | Cerebral arteriopathy |
Variation | info |
Gene | HTRA1 |
CLNDBN | Cerebral arteriopathy, autosomal dominant, with subcortical infarcts and leukoencephalopathy, type 2 |
Reversed | 0 |
HGVS | NC_000010.10:g.124248442G>T |
CLNSRC | OMIM Allelic Variant |
CLNACC | RCV000206925.2, |