rs1789953
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs1789953(C;T) |
Make rs1789953(T;T) |
Reference | GRCh38.p2 38.2/146 |
Chromosome | 21 |
Position | 43062826 |
Gene | CBS |
is a | snp |
is | mentioned by |
dbSNP | rs1789953 |
dbSNP (classic) | rs1789953 |
ClinGen | rs1789953 |
ebi | rs1789953 |
HLI | rs1789953 |
Exac | rs1789953 |
Gnomad | rs1789953 |
Varsome | rs1789953 |
LitVar | rs1789953 |
Map | rs1789953 |
PheGenI | rs1789953 |
Biobank | rs1789953 |
1000 genomes | rs1789953 |
hgdp | rs1789953 |
ensembl | rs1789953 |
geneview | rs1789953 |
scholar | rs1789953 |
rs1789953 | |
pharmgkb | rs1789953 |
gwascentral | rs1789953 |
openSNP | rs1789953 |
23andMe | rs1789953 |
SNPshot | rs1789953 |
SNPdbe | rs1789953 |
MSV3d | rs1789953 |
GWAS Ctlg | rs1789953 |
Max Magnitude | 0 |
? | (C;C) (C;T) (T;T) | 28 |
---|---|---|
|
[PMID 26955774] The association of single nucleotide polymorphisms of the maternal cystathionine-β-synthase gene with early-onset preeclampsia.
ClinVar | |
---|---|
Risk | rs1789953(T;T) |
Alt | rs1789953(T;T) |
Reference | Rs1789953(C;C) |
Significance | Non-pathogenic |
Disease | not specified |
Variation | info |
Gene | CBSL CBS |
CLNDBN | not specified |
Reversed | 0 |
HGVS | NC_000021.8:g.44482936C>T |
CLNSRC | |
CLNACC | RCV000198954.1, |