rs587776446
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs587776446(C;T) |
Make rs587776446(T;T) |
Reference | GRCh38 38.1/142 |
Chromosome | 10 |
Position | 122506767 |
Gene | HTRA1 |
is a | snp |
is | mentioned by |
dbSNP | rs587776446 |
dbSNP (classic) | rs587776446 |
ClinGen | rs587776446 |
ebi | rs587776446 |
HLI | rs587776446 |
Exac | rs587776446 |
Gnomad | rs587776446 |
Varsome | rs587776446 |
LitVar | rs587776446 |
Map | rs587776446 |
PheGenI | rs587776446 |
Biobank | rs587776446 |
1000 genomes | rs587776446 |
hgdp | rs587776446 |
ensembl | rs587776446 |
geneview | rs587776446 |
scholar | rs587776446 |
rs587776446 | |
pharmgkb | rs587776446 |
gwascentral | rs587776446 |
openSNP | rs587776446 |
23andMe | rs587776446 |
SNPshot | rs587776446 |
SNPdbe | rs587776446 |
MSV3d | rs587776446 |
GWAS Ctlg | rs587776446 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs587776446(T;T) |
Alt | rs587776446(T;T) |
Reference | Rs587776446(C;C) |
Significance | Other |
Disease | Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy |
Variation | info |
Gene | HTRA1 |
CLNDBN | Cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy |
Reversed | 0 |
HGVS | NC_000010.10:g.124266283C>T |
CLNSRC | ClinVar |
CLNACC | RCV000144148.1, |