rs138211175
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs138211175(C;T) |
Make rs138211175(T;T) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 21 |
Position | 43058919 |
Gene | CBS |
is a | snp |
is | mentioned by |
dbSNP | rs138211175 |
dbSNP (classic) | rs138211175 |
ClinGen | rs138211175 |
ebi | rs138211175 |
HLI | rs138211175 |
Exac | rs138211175 |
Gnomad | rs138211175 |
Varsome | rs138211175 |
LitVar | rs138211175 |
Map | rs138211175 |
PheGenI | rs138211175 |
Biobank | rs138211175 |
1000 genomes | rs138211175 |
hgdp | rs138211175 |
ensembl | rs138211175 |
geneview | rs138211175 |
scholar | rs138211175 |
rs138211175 | |
pharmgkb | rs138211175 |
gwascentral | rs138211175 |
openSNP | rs138211175 |
23andMe | rs138211175 |
SNPshot | rs138211175 |
SNPdbe | rs138211175 |
MSV3d | rs138211175 |
GWAS Ctlg | rs138211175 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs138211175(T;T) |
Alt | rs138211175(T;T) |
Reference | Rs138211175(C;C) |
Significance | Probable-Pathogenic |
Disease | not provided |
Variation | info |
Gene | CBS |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.44479029C>T |
CLNSRC | |
CLNACC | RCV000200590.1, |