rs762065361
From SNPedia
Orientation | plus |
Stabilized | plus |
Geno | Mag | Summary |
---|---|---|
(C;C) | 0 | common in clinvar |
Make rs762065361(A;A) |
Make rs762065361(A;C) |
Reference | GRCh38.p2 38.2/147 |
Chromosome | 21 |
Position | 43065621 |
Gene | CBS |
is a | snp |
is | mentioned by |
dbSNP | rs762065361 |
dbSNP (classic) | rs762065361 |
ClinGen | rs762065361 |
ebi | rs762065361 |
HLI | rs762065361 |
Exac | rs762065361 |
Gnomad | rs762065361 |
Varsome | rs762065361 |
LitVar | rs762065361 |
Map | rs762065361 |
PheGenI | rs762065361 |
Biobank | rs762065361 |
1000 genomes | rs762065361 |
hgdp | rs762065361 |
ensembl | rs762065361 |
geneview | rs762065361 |
scholar | rs762065361 |
rs762065361 | |
pharmgkb | rs762065361 |
gwascentral | rs762065361 |
openSNP | rs762065361 |
23andMe | rs762065361 |
SNPshot | rs762065361 |
SNPdbe | rs762065361 |
MSV3d | rs762065361 |
GWAS Ctlg | rs762065361 |
Max Magnitude | 0 |
ClinVar | |
---|---|
Risk | rs762065361(A;A) |
Alt | rs762065361(A;A) |
Reference | Rs762065361(C;C) |
Significance | Pathogenic |
Disease | not provided |
Variation | info |
Gene | CBSL CBS |
CLNDBN | not provided |
Reversed | 0 |
HGVS | NC_000021.8:g.44485731C>A |
CLNSRC | |
CLNACC | RCV000200013.1, |